Title of Invention

ECTOPARASITICIDAL SPOT-ON FORMULATIONS COMPRISING FIPRONIL AND AMITRAZ

Abstract

The present invention provides a parasiticidal spot-on formulation for the treatment or prevention of parasite infestations in non-human mammals or birds comprising an ectoparasiticidal combination comprising of fipronil and amitraz; a pharmaceutical or veterinary acceptable liquid carrier vehicle for applying the formulation to a localized region on an animal comprising a solvent and optionally a cosolvent and optionally, a crystallization inhibitor. The inventive formula remains effective up to three months from the first application. Moreover, the inventive formulations prevent tick attachment to the animal, thereby providing protection against tick borne diseases. The ectoparasites which may be controlled, treated or prevented by the present invention includes ticks, fleas, mites, mange, lice, mosquitoes, flies and cattle grubs.

Full Text

The application claims priority from US provisional application USSN 60/530.525, filed December 17, 2003, and US Utility application USSN 10/783,459. filed February 20, 2004, herein incorporated by reference, together with each document cited therein. Reference is also made to application USSN 10/374,627 filed February 26, 2003, entitled 1-N-arylpyrazole Derivatives in Prevention of Arthropod-Borne and Mosquito-Borne Diseases. This application and all applications and prior publications cither therein (including documents cited in the text or during prosecution) and all documents cited herein ("appln cited documents") and all documents cited or referenced in appln cited documents are hereby expressly incorporated by reference. FIELD OF THE INVENTION This invention provides for, inter alia, novel topical formulations comprising at least one 1-N-arylpyrazole derivatives and at least one formamidine such as amitraz and to methods for treating parasite infestations in mammals and birds by topically applying the inventive formulations to said mammals and birds. The inventive formulations exhibit activity against ectoparasites such as fleas and ticks, that is far superior than formulations comprising an 1-N-arypyrazole derivative alone, such as fipronil, thereby indicating synergy. This result is even more surprising given the fact that amitraz is not recognized in the field as a flea product. BACKGROUND OF THE INVENTION Parasitic diseases may be caused by either endoparasites or ectoparasites. As used herein endoparasites refer to those parasites living inside the body of the host, either within an organ (such as the stomach, lungs, heart, intestines, etc.) or simply under the skin. Ectoparasites are those parasites that live on the outer surface of the host but still draw nutrients from the host. Endoparasitic diseases may further be subdivided based on class of parasite involved in the infection. For example, endoparasitic diseases generally referred to as helminthiasis are due to infection of the host with parasitic worms known as helminths. Helminthiasis is a prevalent and serious worldwide economic problem involving infection of domesticated animals such as swine, sheep, horses, cattle, goats, dogs, cats, and poultry. Many of these infections, caused by the group of worms described as nematodes, cause diseases in various species of animals throughout the world. These diseases are frequently serious and can result in the death of the infected animal. The most common genera of nematodes infecting the animals referred to above include, but are not limited to, Haemonchus, Trichostrongylus, Ostertagia, Nematodirus, Cooperia, Ascaris, Bunostomum, Oesophagostomum, Chabertia, Trichuris, Strongylus, Trichonema, Dictyocaulus, Capillaria, Heterakis, Toxocara, Ascaridia, Oxyuris, Ancylostoma, Uncinaria, Toxascaris, and Parascaris. Many parasites are species specific (infect only one host) and most also have a preferred site of infection within the animal. Thus, Haemonchus and Ostertagia primarily infect the stomach while Nematodirus and Cooperia mostly attack the intestines. Other endoparasites reside in the heart, eyes, lungs, blood vessels, and the like while still others are subcutaneous parasites. Helminthiasis can lead to weakness, weight loss, anemia, intestinal damage, malnutrition, and damage to other organs. If left untreated these diseases can result in the death of the animal. Examples of endoparasites which infect animals and man include but are not limited to gastro-intestinal parasites of the genera Ancylostoma, Necator, Ascaris, Strongyloides, Trichinella, Capillaria, Trichuris, Enterobius, and the like. Other endoparasites which intect animals and man are found in the blood or in other organs. Examples of such parasites include but are not limited to filarial worms Wuchereria, Brugia, Onchocerca, and the like as well as extra-intestinal stages of the intestinal worms Strongylides and Trichinella. Ectoparasites which infest man and domestic animals include arthropods, such as ticks, fleas. mites, mosquitos, lice, and the like and infections by these parasites can result in transmission of serious and even fatal diseases. Infestations by ectoparasitic arthropods including but not limited to ticks, mites, lice, stable flies, hornflies, blowflies, face fies, fleas, mosquitoes and the like are also a serious problem. Infection by these parasites results not only in loss of blood and skin lesions, but also can interfere with normal eating habits thus causing weight loss. Ectoparasitic infestations of a host can also result in transmission of serious diseases including but not limited to encephalitis, anaplasmosis, babesiosis, rocky mountain spotted fever, Lyme disease, ehrlichiosis, West Nile virus, swine pox, malaria, yellow fever, and the like, many of which can be fatal to the host. Animals may be infected by several species of parasite at the same time since infection by one parasite may weaken the animal and make it more susceptible to infection by a second species of parasite. Many of the compounds used in this invention are also active against household pests including but not limited to cockroach, Blatella sp., clothes moth, Tineola sp., carpet beetle, Allagenus sp. and the housefly Musca clomeslica and against Solenopsis invicta (imported fire ants), termites, and the like. These compounds are furthermore useful against agricultural pests such as aphids (Acyrthiosiphon sp.) locusts, and boll weevils as well as against insect pest which attack stored grains such as Tribolium sp. and against immature stages of insects living on plant tissue. Anthelmintic compounds are also useful as a nematodicide for the control of soil nematodes, which may be agriculturally important. Antiparasitic agents are also useful for the treatment and/or prevention of helminthiasis in domestic animals such as cattle, sheep, horses, dogs, cats, goats, swine, and poultry. They are also useful in the prevention and treatment of parasitic infections of these animals by ectoparasites such as ticks, mites, lice, fleas, mosquitoes and the like. They are also effective in the treatment of parasitic infections of humans. Various methods of formulating antiparasitical formulations are known in the art. These include oral formulations, baits, dietary supplements, powders, shampoos, etc. Formulations for localized topical applications of antiparasitical formulations are also known in the art. For example, pour-on solutions comprising 1-N-phenylpyrazole derivatives, such as fipronil, are known in the art and are described in, for example. U.S. Patent 6,010,710, U.S. Patent 6,413,542, U.S. Patent No. 6,001,384, U.S. Patent 6,413,542 as well as copending application 10/120,691, filed April 11, 2002 and now allowed. Other methods of formulating antiparasitic agents include spot-on formulations or spays. Spot-on formulations are well known techniques for topically delivering an antiparasitic agent to a limited area of the host. For example, U.S. Patent 5,045,536 describes such formulations for ectoparasites. Other spot-on formulations include U.S. Patent 6,426,333 and U.S. Patent 6,482,425 and application USSN 10/155,397, now allowed and published as Publication No. U.S. 2003-0050327A1. Reference is also made to Publication No. U.S. 2003-166688A1. WO 01/957715 describes a method for controlling ectoparasites in small rodents as well as interrupting or preventing the diseases caused by arthropods or small rodents, which comprise applying topical formulations, such as spot-on compositions, to the skin, or hair of the rodents. l-N-arylpyrazoles as a class of chemicals are well known in the art, as well as methods for their use in controlling parasites including insects, such as fleas, ticks, lice or mosquitoes in mammals, such as domesticated livestock or companion animals or birds, either alone or in combination with other pesticides such as insect growth regulators. See, e.g.. EP-A-295,217, EP 295 177, EP-A-840-686, EP-A-352,944, WO 00/35844, WO 98/39972. U.S. Patent Nos. 5,122.530 5,236,938, 5,232,940, 5,576,429 5,814,652, 5,567.429. 6,090,751 and 6,096,329 as \\ell as Publication No. US 2002-90381-A I. Sec also copending applications USSN 07/719,942; 08/933,016; 09/174,598; 08/863,182; and 08/863,692. The compounds of the families defined in these patents are extremely active and one of these compounds, 5-amino-3-cyano-l-(2,6-dichloro-4-tritluoromethylphenyl)-4-trifluoromethylsulfinylpyrazole, or fipronil, is particularly effective, but not exclusively effective, against fleas and ticks. The I -arylpyrazoles exert their activity by being distributed through the sebaceous glands of the animal. WO-A-87/3781, EP-A-295,117 and EP-A-500,209 describe a class of insecticides which are N-phenyl-pyrazole derivatives. These compounds are given as having activity against a very large number of parasites, including insects and acarines in fields as varied as agriculture, public health and veterinary medicine. The general teaching of these documents indicates that these insecticidal compounds may be administered via different routes: oral, parenteral, percutaneous and topical routes. Topical administration comprises, in particular, skin solutions (pour-on or spot-on), sprays, drenches, baths, showers, jets, powders, greases, shampoos, creams, etc. The pour-on type skin solutions may be designed for percutaneous administration. Example 9 of EP-A-295.117 and Example 291 of EP-A-500,209 describe a pour-on type skin solution containing 15% insecticide and 85% dimethyl sulphoxide, for percutaneous administration of the insecticide. 1-N-arylpyrazole derivatives are known in the art to prevent, treat or control ectoparasite infestation in mammals, such as cats, dogs and cattle. Amitraz is known in the art as a pesticide and is used to control red spider mites, leaf mites, scale insects and aphids. In animals, amitraz is used to control tick, mites, and lice. Extoxnet http://ace.orst.edu/info/extonet/pips/amitraz.html. However, amitraz is not known in the art to treat fleas Amitraz belongs to the formamidine chemical group, a group including chlordimeform and chlormebuform, both of which are useful in crop protection. Amitraz. described in U.S. Patent Nos. 3.781.355 and 3,864,497 (the contents of which are hereby incorporated by reference in their entireties) has the following structure. (Figure Removed)Other compounds that are known in the art to present, treat or control endo- and ectoparasite infestation include milbemycin or avermectin derivatives. The avermectin and milbemycin series of compounds are potent anthelmintic and antiparasitic agents against a wide range of internal and external parasites. The compounds which belong to this series are either natural products or are semi-synthetic derivatives thereof. The structures of these two series of compounds are closely related and they both share a complex 16-membered macrocyclic lactone ring; however, the milbemycin do not contain the aglycone substituent in the 13-position of the lactone ring. The natural product avermectins are disclosed in U.S. Patent 4.310,519 to Albers-Schonberg, et al., and the 22, 23-dihydro avermectin compounds are disclosed in Chabala, et al., U.S. Patent 4,199,569. For a general discussion of avermectins, which include a discussion of their uses in humans and animals, see "Ivermectin and Abamectin," W.C. Campbell, ed.. Springer-Verlag, New York (1989). Naturally occurring milbemycins are described in Aoki et al., U.S. Patent 3,950,360 as well as in the various references cited in "The Merck Index" 12th ed., S. Budavari. Ed.. Merck & Co., Inc.Whitehouse Station. New Jersey (1996). Semisynthetic derivatives of these classes of compounds are well known in the an and are described, for example, in U.S. Patent 5.077,308. U.S. Patent 4,859,657. U.S. Patent 4,963,582, U.S. Patent 4.855,317, U.S. Patent 4.871.719. U.S. Patent 4,874,749, U.S. Patent 4.427,663, U.S. Patent 4.310,519, U.S. Patent 4.199,569. U.S. Patent 5,055,596, U.S. Patent 4,973,711, U.S. Patent 4.978,677, and U.S. Patent 4.920,148. Avermectins and milbemycins share the same common 16-membered macrocyclic lactone ring; however, milbemycins do not possess the disaccharide substituent on the 13-posilion of the lactone ring. While many avermectin compounds are known in the art, a representative structure of the class of compounds is as follows (Figure Removed)where the broken line indicates a single or a double bond at the 22,23-positions: RI is hydrogen or hydroxy provided that RI is present only when the broken line indicates a single bond; (Figure Removed) R2 is alkyl of from I to 6 carbon atoms or alkenyl of from 3 to 6 carbon atoms or cycloalkyl of from 3 to 8 carbon atoms: Rj is hydroxy, metho\\ or = NORs where Rj is hydrogen or lower alky I: and Ra is hydrogen, hydroxy or (Figure Removed)where R& is hydroxy, ami no, mono-or di-lower alkylamino or lower alkanoylamino. The preferred compounds are avermectin Bla/BIb (abamectin), 22,23-dihydro avermectin Bla/BIb (ivermectin) and the 4"-acetylamino-5-ketoximino derivative of avermectin Bla/BIb. Both abamectin and ivermectin are approved as broad spectrum antiparasitic agents. The structures of abamectin and ivermectin are as follows:(Figure Removed)wherein for abamectin the broken line represents a double bond and RI is not present and for ivermectin the double bond represents a single bond and R, is hydrogen: and RT is isopropyl or sec-butyl. The 4"-acetyl amino-5-ketoximino derivatives of avermectin Bla/Blb has the followin« structural formula:(Figure Removed)where R? is isopropyl or sec-butyl. The avermectin products are generally prepared as a mixture of at least 80% of the compound where R2 is sec-butyl and no more than 20% of the compound where Ri is isopropyl. Other preferred avermectins, include emamectin, eprinomectin and doramectin. Doramectin is disclosed in U.S. Patent 5,089.490 and EP 214 738. This compound has the following structure:In the present formulations, ivermectin and eprinomectin are especially preferred. A representative structure for a milbemycin is that for milbemycin a\: An especially preferred avermectin is moxidectin, whose structure is as followsThe compound is disclosed in U.S. Patent No. 5,089,490. Other classes of compound are known to treat endo-and ectoparasites. These classes include benzimidazoles, which are effective against tapeworms, lungworms and round\\orms,iinida/.othiazoles, which are effective against roundworms. tapeworms and lungworms. and the p>rethroids. Examples of benzimida/oles inclcude albendazole (U.S. Patent 3.915.986): fenbenzazole (U.S. 3.954,791). mebendazole (U.S. 3,657,261). oxibenzazole (U.S. 3.574.845) and triclabenzazole (U.S. 4.197.307). An example of an imidazothiazole is levamisole(U.S. 3.529,350). The pyrethoids are a class of naturally occurring or synthetically derived insecticide. Synthetic pyrethroids include pyrethrin 1 and pyrethrin II. Synthetic pyrethroids include permethrin (U.S. Patent 4,113,968), resmethrin, and sumithrin (U.S. Patents 3,934,023 and 2,348,930), deltamethrin and fenvalerate. SUMMARY OF THE INVENTION The present invention provides for, inter alia, novel topical formulations comprising at least one 1-N-arypyrazole derivative and a formamidine, such as but not limited to amitraz, and to methods for treating, controlling, or preventing parasite infestations on mammals or birds The inventive formulations include spot-on, pour-on or spray formulations and may include a further ectoparasiticide, such as an IGR compound, an avermectin or milbemycin derivative, or a pyrethroid insecticides, and anthelmintics, such as benzimidazoles and imidazothiazoles. The inventive formulation provides a larger duration of parasite control at a faster rate of control. The inventive formula remains effective up to three months from the first application. Moreover, the inventive formulations prevent tick attachment to the animal, thereby providing protection against tick borne diseases. The ectoparasites which may be controlled, treated or prevented by the present invention includes ticks, fleas, mites, mange, lice, mosquitoes, flies and cattle grubs.More specifically, the present invention provides for. inter alia, a parasitical spot-on formulation, which comprises: a) an effective amount of an ectoparasitical combination comprising an 1- N-arylpyrazole derivative and a formamidine: b) a pharmaceutical or veterinary acceptable liquid carrier vehicle: c) optionally, a crystallization inhibitor. This invention further provides fora parasitical pour-on formulation, which comprises: a) an effective amount of an ectoparasitical combination comprising an 1- N-arylpyrazole derivative and amitraz; b) a pharmaceutical or veterinary acceptable liquid carrier vehicle; c) optionally, a crystallization inhibitor; and d) optionally, an antioxidant. Also provided for in the present invention is a parasitical spray formulation, which comprises: a) an effective amount of an ectoparasitical combination comprising an 1- N-arylpyrazole derivative and amitraz: b) a pharmaceutical or veterinary acceptable liquid carrier vehicle. A further embodiment of the present invention are spot-on, pour-on or spray formulations that further comprise at least one additional antiparasiticidal or anthelmintic agent, such as an IGR compound, a milbemycin or avermectin derivative, a pyrethroid, a benzimidazole. such as albendazole, fenbenzazole, mebendazole, oxibendazole, or triclobendazole, or a imidazothiazole, such as levamisole. The present invention further provides for a method for preventing, eliminating or controlling parasites in a mammal or bird in need thereof or an environment where they reside, which comprises applying an effective amount of the inventive spot-on, pour-on or spray formulation to the mammal or bird. Animals include mammals, such as dog, cats, zebras and horses, and birds, such as chickens, turkeys and quail. Environments include animal houses, such as dog or cat bedding, horse stables and chicken litter. DETAILED DESCRIPTION OF THE INVENTION Other objects, features and aspects of the present invention are disclosed in, or are obvious from, the following Detailed Description. It is to be understood by one of ordinary skill in the art that the present discussion is a description of exemplary embodiments only and is not intended as limiting the broader aspects of the present invention, which broader aspects are embodied in the exemplary construction. In fact, it will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. For instance, features illustrated or described as part of one embodiment can be used in another embodiment to yield a still further embodiment. It is intended that the present invention cover such modifications and variations as come within the scope of the appended claims and their equivalents. For convenience, certain terms employed in the Specification. Examples, and appended Claims are collected here. Definitions: As used herein, the term "comprising" in this disclosure can mean "including" or can have the meaning commonly given to the term "comprising" in U.S. Patent Law. Preferred topical formulations include those formulations wherein the 1-arylpyrazol is a compound of the formula:(Figure Removed)in which: RI is a halogen atom, CN or alkyl; R? is S(O)nR;, or 4,5-dicyanoimidazo!-2-yl or haloalkyi; Rj is alkyl, alkenyl, alkynyl, haloalkyi, haloalkenyl or haloalkyi; R4 is hydrogen, halogen, NR5R6, S(O)mR7- C(O)R7, C(O)OR7, alkyl, haloalkyi , OR« or-N=C(R9)(Rio) substituent; RS and R& independently represent a hydrogen atom, alkyl, haloalkyi, C(O)aIkyl, S(O)rCF3 or alkoxycarbonyl or R? and R6 together may combine to form a ring of 5 to 7 members. R7 represents an alkyl or haloalkyi group; RH represents an alkyl, haloalkyi or a hydrogen; R9 represents an alkyl or a hydrogen; R 10 represents an optionally substituted aryl or an optionally substituted heteroaryl group; RH and R|2 represent, independently of one another, hydrogen. halogen CN or NO2; Ri3 represents a halogen atom or a haloalkyi, haloalkoxy, S(O) or SF? group: in. n. q and r represent, independently of one another, an integer equal to I or2: X represents a trivalent nitrogen atom or a C-R|2, the three other valencies of the carbon atom forming part of the aromatic ring optionally with a pharmaceutically acceptable carrier or excipient. A more preferred formulation is one wherein the 1-N-arylpyrazole is a compound of the formula:(Figure Removed)in which: RI is a halogen atom, CN or methyl; Ri is S(O)nR3 or 4,5-dicyanoimidazol-2-yl or haloalkyl; R3 is alkyl, haloalkyl, haloalkenyl or haloalkynyl; R4 represents a hydrogen or halogen atom or an NRsRd, S(O)mR7, C(O)R7 or C(O)OR7, alkyl, haloalkyl or ORH or an - N=C(Ry)(R|(1) group; R.s and Rf, independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl, S(O)rCF3 or alkoxycarbonyl group or R5 and Rft together may form a ring of 5 to 7 members; R7 represents an alkyl or haloalkyl substitueni; Rx represents an alkyl or haloalkyl or a hydrogen: R9 represents an alkyl or a hydrogen atom: RIO represents an optionally substituted aryl or an optionally substituted heteroaryl group; RM and R|2 represent, independently of one another, hydrogen. halogen CN or NCb; Ri3 represents a halogen atom or a haloalkyl, haloalkoxy, S(O),,CF3 or SF.s group: m, n, q and r represent, independently of one another, an integer equal toO, I or2: X represents a trivalent nitrogen atom or a C-R|2, the three other valencies of the carbon atom forming part of the aromatic ring; with the proviso that, when RI is methyl, then either R3 is haloalkyl, R4 is NH2, RH is Cl, RI:, is CF3 and X is N or else R2 is 4,5-dicyanoimidazol-2-yl, R4 is Cl, RI i is Cl, R,3 is CF3 and X is C-CI; and/or More preferably, this invention provides for a parasitical spot-on formulation wherein the 1-N-arylpyrazole in the ectoparasitical combination is a compound of the formula (1) wherein:RI is a halogen atom, CN or methyl; R2 is S(O)nR:, or 4,5-dicyanoimidazol-2-yl or haloalkyl; R3 isC|-C,,.alkyl or C|-C6-haloalkyl; R4 represents a hydrogen or halogen atom; or NR.sR(,, S(0)mR7, C(O)R7 or C(O)OR7, alkyl, haloalkyl or OR* or -N=C(Ry) (Rio): R5 and R6 independently represent a hydrogen atom or a Ci-C6 alkyl, Ci-CVhaloalkyl. C(O)CrC6-alkyl, S(O)rCF3. C,-C6-acyl or C,-C6-alkoxycarbonyl; R5 and R6 together may combine to form a ring of 5 to 7 members, which may include one or two divalent heteroatoms selected from the group consisting of oxygen or sulphur; Ry represents a C|-C6-alkyl or Ci-Ce-haloalkyl: RS represents a Ci-C6-alkyl or C|-C6-haloalkyl or a hydrogen atom; Rg represents a C|-C6-alkyl or a hydrogen atom; RIO represents an optionally substituted phenyl or optionally substituted heteroaryl group wherein the substituents are selected from the group consisting of halogen, OH, -O- C]-C6 alky I, -S- C i -C6-alkyl, cyano or C i -C6-alky 1; RII and R|2, independently of one another represent hydrogen, halogen, CN or NO2; RIB represents a halogen, C|-Cft-haloaIkyl, CVC6-haloalkoxy, S(O)qCl3 or SF? group; and, m, n, q and r independently of one another are 0, 1, or 2; (b) the liquid carrier vehicle comprises a solvent and a cosolvent wherein the solvent is selected from the group consisting of acetone, acetonitrile, benzyl alcohol, butyl diglycol, dimethylacetamide, dimethylformamide, dipropylene glycol n-butyl ether, ethylene glycol monoethyl ether, monomethylacetamide, dipropylene glycol monomethyl ether, liquid poiyoxyethylene glycols, propylene glycol, 2-pyrroIidone, in particular N-methylpyrrolidone, diethylene glycol monoethyl ether, ethylene glycol, diethyl phthalate fatty acid esters, such as the diethyl ester or diisobutyl ad Spate, and a mixture of at least two of these solvents and the cosolvent is selected from the group consisting of ethanol. isopropanol or methanol; and (c) a crystallization inhibitor selected from the group consisting of an anionic surfactant, a cationic surfactant, a non-ionic surfactant, an amine salt, an amphoteric surfactant or polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol. sorbitol. polyoxyethylenated sorbitan esters; lecithin, sodium carboxymethylcellulose, and acrylic derivatives, or a mixture of these crystallization inhibitors. Especially preferred as spot-on formulations are those wherein the 1-N-arylpyrazole derivative in the ectoparasitical combination is a compound wherein the ring formed by the divalent alkylene substituent representing RO and R6 and the nitrogen atom to which Rs and R(l are attached has 5, 6 or 7 members or wherein RI is CM, R3 is CpCVhaloalkyl. R4 is NH2, RII and Ri2 are, independently of one another, hydrogen or halogen and R|3 is CrC(,-haloalkyl. Most especially preferred 1-N-arylpyrazoles to be used in the inventive spot-on and pour-on formulations are: (A) 5-aiT)ino-3-cyano-l-(2,6-dichloro-4-trifluoromethylphenyl)-4- trifluoromethylsulfinylpyrazole; or (B) 1-N-phenylpyrazole derivative of the formula: (Figure Removed)Other l-N-arylpyrazole derivatives to be used in the formulation to the invention which are preferred are those of the formula (II) wherein: RIOI is cyano. -C(O)alkyl, C(S)NH2, alkyl, haloalkyl, C(=NOH)NH2 orC(=NNH2)NH2; Riu2 is S(O)n RIO:,, alkenyl, haloalkenyl, cycloalkyl, halocycloalkyl or alkynyl: RKO is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl or haloalkynyl; Rio4 is -N=C(Ri«5)-Z-R,o6, -N=C(Rl(,.0-N(Rln7)-RioK; or-N(R,(W)-C(R|(,5)=NR|U6; RIOS is hydrogen; alkyl; or alkyl substituted by halogen, alkoxy, haloalkoxy or -S(O)m-Rio5; Rn)6 and Run each independently represent hydrogen, alkyl, alkenyl or alkynyl, or alkyl substituted by one or more halogen, alkoxy, haloalkoxy, ami no, alkylamino, dialkylamino, cyano or -S(O)m RH?: or alkyl substituted by phenyl or pyridyl each of which is optionally substituted with one or more groups selected from halogen, nitro and alkyl group; orRlov and R|,,s ma\ lorm together with the nitrogen to which they are attached a 3- to 7- membered ring which may additionally contain one or more heteroatoms selected from oxygen. nitrogen or sulfur: RIDS is alkoxy. lialoalkoxy, amino, alkylamino. dialkylamino, -C'(O) Rii4or-S(O),RIM); Rum, Rnoand Riuare alkyl or haloalkyl; RIM and RUT are independently selected from halogen, hydrogen, CN and NO2 Rin is selected from halogen, haloalkyl, haloalkoxy, -S(O)q and -SF5; Rii5 is alkyl or haloalkyl; X is selected from nitrogen and C-R| 12; Z isO, S(O)u:orNR|()7; a', m\ n' and q' are independently selected from 0, 1, and 2; and t' is 0, I or 2; and veterinary acceptable salts thereof. Other preferred 1-N-arylpyrazole derivatives that may be included in the inventive formulations are those compounds of formula (III): wherein:R2l,i is cyano, C(O)alkyl, C(S)NH2, alkyl, C(=NOH)NH2 or C(=NNH2)NH2; R202 is S(O)hR20:,, alkenyl, haloalkenyl, cycloalky!, halocycloalkyl or alkynyl; R203 is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl or haloalkynyl; R204 is -N(R2,)5)C(O)CR206R207R208, -N(R205)C(0)aryl. or -N(R2os)C(O)OR2l)7; Rios is alkyl, haloalkyl, cycloalkyl, halocycloalkyl. cycloalkylalkyl. halocycloalkylalkyl, alkoxyalkyl, haloalkoxyalkyl, alkenyl, haloalkenyl, alkynyl, haloalkynyl; R2o6 is hydrogen, halogen, alkoxy, haloalkoxy, alkoxyalkyl, haloalkoxyalkyl. tbrmyloxy, alkylcarbonyloxy, haloalkylcarbonyloxy, alkylthio, haloalkylthio, alkylsulfmyl, haloalkylsulfinyl, alkylsulfonyl, haloalkylsulfonyl, alkylamino, dialkylamino. haloalkylamino, di(haloalkyl)amino, cycloalkyloxy. halocycloalkyloxy, alkoxyalkoxy, haloalkox) ulkoxy, alkoxyalkoxyalkoxy, aryloxy. or arylalkoxy; R207 and R^xare independently hydrogen, alkyl. haloalkyl. cycloalk\l. orhalocycloalkyl: or R2o?and Riosinay form together with the carbon to uhich they are attached a 3- to 7- membered ring which additionally may contain one or more heteroatoms selected from nitrogen, oxygen and sulfur: Xi is selected from nitrogen and C-R2I2; RTH and R2i2 are independently selected from halogen, hydrogen, CN and NO:; R2n is selected from halogen, haloalkyl, haloalkoxy, -S(O)kCF.i, and -SF5; and h and k are independently selected from 0, 1, and 2; and veterinary acceptable carrier, excipients and salts thereof. A preferred class of compounds of formula (II) for use in the inventive formulation is those wherein: RIUI is cyano or alkyl; Ri02 isS(O),vR,,,v Rio3 is alkyl or haloalkyl; RK,4 is-N=C(Rii,5)-Z-Rio6; RIOS is hydrogen, alkyl or haloalkyl; ZisO.S(O):i-:orNR|()7; RKX, and RIO? are independently selected from hydrogen and unsubstituted or substituted alkyl; or RKKS and RIO? may form together with the nitrogen to which they are attached a 3- to 7- membered ring which may additionallycontain one or more heteroatoms selected from oxygen, nitrogen or sulfur; X is selected from nitrogen and C-R|P_: RIM and R^ are independently selected from halogen, hydrogen. CN and NO:: Rii3 is selected from halogen, haloalkyl, haloalkoxy, -S(O)q-CF:,. and -SF5; a', n' and q' are independently selected from 0. I. and 2. Preferably, R|06 is alkyl which is substituted by one or more halogen, alkoxy, haloalkoxy. amino, alkylamino, dialkylamino, sulfide, sulfoxide, sulfone, or phenyl or pyridyl moieties of which each phenyl or pyridyl moiety is optionally substituted with one or more groups selected from halo, nitro, and alkyl. Preferably, the 1-N-arylpyrazole has one or more of the following features: RIOI is cyano; RUM is -N=CXRm5)-Z-Rio6 and Z is -NRio?; X is C-Ru:; RIM and Rn2 represent a chlorine atom; and RM:, is CF3, OCF;,,or-SF5; R, 12 is -S(O)n CF;, and n is 0, 1, or 2. A further preferred class of 1-N-arylpyrazoles that may be included in the inventive formulations or approaches are those of formula II wherein: RIOI is cyano or alkyl; RUM is -N=C(R|05)-Z-R|06; and RIO.S is hydrogen or Ci-Cj alkyl. The compounds of formula (II) preferably have one or more of the following features: RIOI is cyano or methyl; RUB is halomethyl (preferably CF3); RIII and RI ,2 each independently represent a halogen atom: X isC-R,i2: RI 13 is haloalk) I (preferably CF3 haloalkoxy (preferably OCF3). or -SF5; or n' is 0, 1 or 2 (preferably 0 or 1). A further preferred class of compounds of formula (II) for use in the inventive formulations and methods are those wherein: RIOI is cyano; Run isS(O)n-R|(l.i: Rio3 is halomethyl; Ri,)4 is-N=C(R|()5)-Z-R|l)fi; Z isNR|()7; RIOS is hydrogen or alkyl; Rio6 and RIO? each independently represent hydrogen, alkyl, alkenyl or alkynyl; or alkyl substituted by one or more halogen, alkoxy, haloalkoxy. amino, alkylamino, dialkylamino, cyano or -S(O)mR|s; or alkyl substituted by phenyl or pyridyl which rings are optionally substituted with one or more groups selected from halogen, nitro and alkyl; X is selected from nitrogen and C-R| 12; RHK, and RH: each independently represent a halogen atom; RH:, is selected from haloalkyl, haloalkoxy and -SF..; RU? is alkyl or haloalkyl: and m' and n' are independently selected from 0, 1, and 2. A further preferred class of compounds of formula (II) is that wherein: RIIII is cyano: RUG is$(O)nCT:,: RUM is -N=C(R,(,,)-Z-R|06 or -N=C(R|,,5)-N(RM,,)-RI08: Z isNR|()7: RIDS is hydrogen or alkyl; Rio6 and R|(,7 each independently represent hydrogen, alkyl, alkenyl or alkynyl; or alkyl substituted by one or more halogen, alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, cyano or -S(O)Rns; or methyl substituted by phenyl or pyridyl which rings are optionally substituted with one or more groups selected from halogen, nitro and alkyl; RIOS is alkoxy, haloalkoxy, amino, alkylamino. dialkylamino or X is selected from nitrogen and C-R| 12; Rio9, RIIO and RM4 independently represent alkyl or haloalkyl; Rmand RUT each represent a chlorine atom; Rii3 isCF3or-SF5;and irf and n' are 0, I or 2; and t' is 0 or 2. A further preferred class of compounds of formula (II) are those wherein; RIOI is cyano; R,,12 isS(0)n,Ch: RIM is-N=C(Riu5)-Z-Rn«,; Z isNR|,,7: RIOS is hydrogen or methyl; Rio(, and R|,|7 each independently represent hydrogen, alkvl. alkenyl or alkynyl: or alky] substituted by one or more halogen, alkoxy. haloalkoxs. amino, alkylamino, dialk\ lamino. cyano or -S(O)m-Rnri: or alkyl substituted by phenyl or pyridyl \\hich rings are optionally substituted with one or more groups selected from halogen, nitro and alkyl; X is C-R|,2 RI 11 and R| 12 each represent a chlorine atom; Rii3 isCF3or-SF5: m' is zero, one or two; and n' is 0 or I. A further preferred class of compounds of formula (II) is those wherein: RIOi is cyano; R,o2 is S(O)n Rio4 is-N=C(R|(l5)-Z-R|06; Z isNR|o7; RIOS and RU)7 each represent a hydrogen atom; RKX, is alkyl or haloalkyl; X isC-Rm; RIII and RI u each represent a chlorine atom; Rin isCF;, or-SF.s; and iV isO. Compounds of formula (III) which are preferred according to the present invention are those wherein: Rioi is cyano: R2()2 is R2(,3 is alkyl or haloalkyl: R:,,4 is - RIDS is alkyl, haloalkyl, cycloalkyl. cycloalkylalkyl and halocycloalkylalkyl; R206 is alkoxy, haloalkoxy, or hydrogen; R2o7and R^osare independently hydrogen, alkyl, or haloalkyl; or R:o7 and R2()S may form together with the carbon to which they are attached to a 3- to 7- membered ring which additionally may contain one or more heteroatoms selected from nitrogen, oxygen and sulfur; X| is selected from nitrogen and C-R2!2; R2n and R2|2 are independently selected from halogen, hydrogen, CN and NO2; R2n is selected from halogen, haloalkyl, haloalkoxy. -S(O)kCF-i, and SF5; and h and k are independently selected from 0, I, and 2. A preferred group of compounds of formula (III) is that wherein the ring which is formed by R2()7and R2()scontains one or more heteroatoms, more preferably one oxygen atom. The compounds of formula (111) of the present invention preferably have one or more of the following features: R2oi is cyano: R203 is halometliyl. preferably CF3; R2n and R2[2are independently halogen; X| is C-R2i2: R2n is haloalkyl. haloalkoxy or -SF,: or h is 0 or I. or 2. preferably 0 or I. A preferred class of compounds that wherein R2()4 is N(R2()5)C(O)CR2.j(lR2()7R2ox. Another preferred class of compounds that wherein R204 is N(R2o.i)C(O)aryl. Another preferred class of compounds that wherein R2o4 is N(R2(I5)C(O)OR207. Preferably R2(15 is C|-C4 alkyl. more preferably C|-C? alkyl, most preferably methyl. Preferably R2()6 is alkoxy, most prelerably methoxy, ethoxy or propoxy. Preferably R2()7and R2osare both hydrogen. Another especially preferred group of l-N-arylpyrazole derivatives is 4-thiocarbonylpyrazole derivatives of the formula: in which RR301 is H2N-C(S)-, 302 is halogenoalkyl. halogenoalkenyl or halogenoalkynyl, 303 is hydrogen, ami no or one of the following groups:where R represents alkyl, halogenoalkyl, alkoxyalkyl or in each case optionally substituted phenyl or pyridyl. R' 3 represents hydrogen or alkyl, R'"1 represents hydrogen, alkyl or in each case optionally substituted phenyl or pyridyl and R"'07 represents alkyl, alkenyl, alkinyl. formyl, alkylcarbonyl, halogenoalkylcarbonyl or alkoxycarbonyl: Ar represents in each case optionally substituted phenyl or pyridyl and n represents a number 0, 1 or 2. Especially preferred derivatives of formula (IV) are those wherein R301 represents H2N-C(S)-; R3U2 preferably represents (C|-C6)-halogenoalkyl having 1 to 12 halogen atoms; (C2-C6)-halogenoalkenyl having I to 8 halogen atoms or (C|-C6)-halogenoalkinyl having 1 to 6 halogen atoms; R3"3 preferably represents hydrogen, amino or one of the following groups:wherein:RM represents (Ci-C())-alkyl, (C|-C6)-halogenoalkyl having I to 3 halogen atoms, (C|-C6)-alkoxy-(C|-C6)-alkyl, or represents phenyl or pyridyl. each of which is optionally monosubstituted to trisubsliiLited by identical or different substituents from the group consisting of cyano, nitro. halogen, C|-C(,-alkyl. C]-C6-alko.\\. C|-C6-alkylthio, C|-C4-halogenoalkyl, C|-C4 halogenoalkoxy or C|-C4-halogenoalkylthio having in each case I to 5 halogen atoms, Rj(b represents hydrogen or (C|-C6)-alkyl, R"'06 represents hydrogen, (C|-C6)-alkyl, phenyl which is optionally monosubstituted to trisubstituted by identical or different substituents from the group consisting of cyano, nitro, halogen, C,-C6-alkyl, C,-C6-alkoxy, C,-C6-alkylthio, C,-C4-halogenoalkyl. C|-C4-halogenoalkoxy or C;-C4-halogenoalkylthio having in each case Ito 5 halogen atoms or hydroxyl, or represents pyridyl which is substituted by cyano, nitro, halogen, C|-C6-alkyl, Ci-C^-alkoxy, C|-C6-alkylthio, C|-C4-halogenoalkyl, C|-C4-halogenoalkoxy or C|-C4-halogenoalkylthio having in each case 1 to 5 halogen atoms, and R3U7 represents (C,-C6)-alkyl, (C2-C6)-alkenyl, (CrC6)-alkynyl. formyl, (C rC(1)-alkylcarbonyl, (C|-Ch)-halogenoalkylcarbonyl having 1 to 6 halogen atoms or (C|-C6)-alkoxycarbonyl; Ar preferably represents phenyl or pyridyl, each of which is optionall\ monosubstituted to trisubstituted by identical or different subslituents from the group consisting of halogen halogeno(C|-C(1)alkyl, halogeno(CrC,,) alkylthio. halogeno(C'i-Ch)alkoxy, (C|-Cft)alkoxy. methoxy. hydrazine, (Ci-C(s)-dialkylhydrazino, amino. (CrC6)alkylamino, di(C|-Cft)alkylamino, (C|-C6) alkylimino, cyano, (Ci-QOalkylihio or the group (Figure Removed)in which RJ° and Rj(W are identical or different and represent hydrogen or (C|-Cft)-alkyl n preferably represents a number 0, I or 2. R301 represents H2N-C(S)-; R302 particularly preferably represents (C|-C_t)-halogenoalkyl having 1 or 9 identical or different halogen atoms from the group consisting of fluorine, chlorine and bromine, (C2-C4)-halogenoalkenyl having 1 to 5 identical or different halogen atoms from the group consisting of fluorine, chlorine or bromine or (CVC4)-halogenoalkynyl having 1 to 5 identical or different halogen atoms from the group consisting of fluorine, chlorine and bromine; RJ°3 especially preferably represents hydrogen, amino or one of the following groups: where RJ°4 represents (C|-C4)-alkyl, (C|-C4)-halogenoalkyl having 1-3 halogen atoms. (C|-C4)-alkoxy(C|-C2)-alkyl. or phenyl which is optionally monosubstituted to trisubstituted by identical or different substituents from the group consisting of hydroxyl, cyano, nitro, halogen, C|-C4-alkyl, C|-C4-alkoxy, (Ci-CVhalogenoalkyl, Ci-C^-halogenoalkoxy or C|-C2-halogenoalkylthio having in each case I to 3 halogen atoms, R3lb represents hydrogen or (CrC4)-alkyl, RJ°6 represents hydrogen, (Ci-C4)-aIkyl or phenyl which is optionally monosubstituted or disubstituted by identical or different substituents from the group consisting of hydroxyl, cyano, nitro, halogen, Ci-C4-alkyl, C|-C4-alkoxy, CVC2-halogenoalkyl, CrC2 halogenoalkoxy or CrC2 halogenoalk) Ithio having in each case 1 to 3 halogen atoms, in particular 4-hydroxy-3-methoxy-phenyl. and R307 represents (C|-C4)-alkyl, (C2-C4)-alkenyl, (C2-C4)-alkynyl. formyl, (CVC4)-alkylcarbonyl, (C|-C4,)-halogenoalkylcarbonyl having 1 to 5 identical or different halogen atoms from the group consisting of fluorine, chlorine or bromine or (CVC.|)-alko\ycarbonyl; Ar especiall) preferably represents phenyl or pyridyl, each of which is optionally monosubstituted to trisubstituted by identical or different substituents from the group consisting of fluorine, chlorine, trifluoromethyl, trifluoromethylthio, trifluoromethoxy, methoxy, hydrazine, dimethylhydrazino, amino, methylamino, dimethylamino, iminomethyl, cyano, methylthio or the group(Figure Removed) where R308 and R3(W are identical or different and represent hydrogen or (d-C4)-alkyl: n"' especially preferably represents a number 0, I or 2. Compounds of formula (IV) which are most preferably preferred are those where R3UI represents H2N-C(S)-; R3"2 most preferably represents one of the following groups: -CF3, -CHF:-CF2-CH3 -CF3-CHF2, -CF2CHFCI, -CH2-CF3. -CH2CF2CI. -CH2-CF2-CHF2, -CF2-CFCI-CF3, -C(CI)(CFj)-CF2CI,-C(C1)(CF3)-CHCI-CF3.-C(CF3)=CCM2 R3()J most preferably represents hydrogen, amino or one of the groups: -NH-CO-CH3, -NH-CO-C2H5, -N=CH-NH2, -N=C(CH3)-NH2, -N=CH-N(CH3)2, -N=C(CH3)-N(CH3)2, -NHC2H5 or -NH-CH2-CH=CH2. Ar most preferably represents (1) phenyl which is disubstituted or trisubstituted by identical or different substituents, where fluorine or chlorine occupies the 2-position. tritluoromethyl the 4-position and fluorine, chlorine, cyano, methoxy, methylthio, trifluoromethyl. trifluoromethoxy, trifluoromethylthio or hydrazino the 6-position; or (2) a 2-pyridyl substituent which is substituted in the 4-position by trifluoromethyl and in the 6-position by fluorine or chlorine. n "' most preferably represents one of the integers 0, I or 2. A most especially preferred compound is one wherein R302 is -CF^, RJ°3 is ammo, Ar is a phenyl which is trisubstituted and the substituents are a 2-position chloro group, a 4-position tritluoromethyl group and a 6-position chloro group, and nmisl. Especially preferred compounds are those of the formulae. (Figure Removed)Especially preferred 1-N-arylpyrazoles derivative in addition to fipronil include fipronil thioand fipronil sulfone In addition to the patent discussing l-N-arylpyrazoles derivatives discussed previously, one skilled in the art could make these compounds by adopting procedures described in DE 19928155, DE 19853560. WO 2000031043, DE 19650197. WO 9824769, US 6265430. US 2001007876, all of which are herein incorporated by reference. The alkyl groups of the definition of the compounds (1) of the formula (1) generally comprise from I to 6 carbon atoms. The ring formed by R5 and R6 and the nitrogen atom to which they are attached is generally a 5-, 6- or 7-membered ring. Unless otherwise specified, alkyl and alkoxy groups are generally lower alkyl and alkoxy groups, that is having from one to six carbon atoms, preferably from one to four carbon atoms. Generally, the haloalkyl. haloalkoxy and alkylamino groups have from one to four carbon atoms. The haloalkyl and haloalkoxy groups can bear one or more halogen atoms; preferred groups of this type include -CF3 and -OCF3. Cycloalkyl groups generally have from 3 to 6 carbon atoms, preferably from 3 to 5 carbon atoms, and may be substituted by one or more halogen atoms. Alkenyl, haloalkenyl, alkynyl, and haloalkynyl groups generally contain from 3 to 5 carbon atoms. By the term aryl is generally meant phenyl, pyridyl, furyl, and thiophenyl, each of which is optionally substituted by one or more halogen, alkyl, haloalkyl, nitro, alkoxy, haloalkoxy, hydroxy, amino, alkylamino or dialkylamino. In compounds of formulae (1) to (111), by the term substituted alkyl is meant alkyl which is substituted by, for example, one or more halogen, alkoxy, haloalkoxy, amino, alkylamino, dialkylamino, cyano or -S(O)mRn5; or alkyl substituted by phenyl or pyridyl each of which is optionally substituted with one or more groups selected from halogen, nitro and alkyl; wherein Rn5 is alkyl or haloalkyl and m is zero, one or two. Preferably in compounds of formula (1), alkyl groups are generally substituted by from one to five halogen atoms, preferably from one to three halogen atoms. Chlorine and fluorine atoms are preferred. Compounds of formula wherein R|,,4 is -N=C(R|(J5)-Z-R|U(1. Z is NR|,)7 and R|U(, represent a hsdrogen atom may exist as ihe tautomeric double bond isomer form -NH-C(R|,M)=N-Rio7. It is to be understood that both such forms are embraced by the present invention. In compounds of formula (III) the following examples of substituents are provided: An example of cycloalkylalkyl is cyclopropylmethyl; an example of cycloalkoxy is cyclopropyloxy; An example of alkoxyalkyl is CH^OCHi-; An example of alkoxyalkoxy is C'l hOCH2O-; An example of alkoxyalkoxyalkoxy is CH3OCH2OCH2O-; An example of aryloxy is the phenoxy group; and An example of the arylalkoxy group is benzyloxy or 2-phenylethoxy. Generally, in dialkylamino or di(haloalkyl)amino groups, the alkyl and haloalkyl groups on nitrogen may be chosen independently of one another. A preferred class of compounds of formula (I) comprises the compounds such that RI is CM, R:, is haloalkyl, R4 is NH2, RU and R!2 are, independently of one another, a halogen atom and R|3 is haloalkyl. Preferably still, X is C-Ri?. A compound of formula (1) which is very particularly preferred in the invention is 5-amino-3-cyano-l-(2,6-dichloro-4-trilluoromethylphenyl)-4-trifluoromethylsLilfinylpyrazole or fipronil. Compounds of formulae (I) - (III) can be prepared according to one or other of the processes described in Patent Applications WO 87/3781, 93/6089 and 94/21606, and 00/59862 or European Patent Application 295,1 17 or any other process coming within the competence of a person skilled in the art who is an expert in chemical synthesis. For the chemical preparation of the products ol'lhe invention, a person skilled in the art is regarded ashaving at his disposal, inter alia, the entire contents of "Chemical Abstracts" and of the documents which are cited therein. As discussed above, amitraz is well known in the art and can be obtained from commercial source. Amitraz belongs lo a chemical group known as the formamidines. Thus, the invention comprehends the use in inventive compositions and methods of at least one formamidine, such as amitraz . h'ormamidines are insecticides having the structure -N=CH-N. such as amitraz, chlordiinetbrm, chlormebuform, formetanate, and l-dimethyl-2-(2'-methyl-4'-chlorophenyl)-formamidine (Chlorphenamidin) that, without wishing to necessarily be bound by any one particular theory, are useful as insecticides by inhibiting monoamine oxidase and/or interfering with an insect's nervous system (eg voltage sensitive gates in nerve membranes) and are especially useful against all stages of mites and ticks. Amounts for application to animals of these insecticides can be determined from known uses of these insecticides, without undue experimentation, (eg, MITABAN is a commercially available amitraz product approved for cattle, swine, and dogs, in the US, typically used as a collar tor dogs, but also available in liquid forms such as a liquid concentrate; amitraz has an oral LD50 in rats of 800 mg/kg, a dermal LD50 in rabbits of >200 mg/kg: when applied to skin of dog in 0.025% solution amitraz produces transient sedation, depression of rectal temperature and increases blood glucose, and amitraz is well tolerated when fed at 0.25 mg/kg/d x 90 days, with, at doses of 1-4 mg/kg hyperglycemia consistently observed, but sedation being the most frequent untoward effect). Accordingly, in inventive compositions and methods, a formamidine, advantageously amitraz, can be emplo)ed, i.e., amitraz is exemplar) of a formamidine that can be used in the invention. Parasiticidal compounds useful in the present invention also include those with an ovicidal and/or larvicidal effect on the immature stages of various ectoparasites. Man)1 of these are already known, for example from patent U.S. Pat. No. 5.439.924. Among these compounds are featured insect growth regulator compounds (1GR) which act either by blocking the development of the immature stages (eggs and larvae) into adult stages, or by inhibiting the synthesis of chitin. Patent FR-A-2,713.889 is moreover known, \\hich generally describes the combination of at least one compound of IGR (insect growth regulator) type, comprising compounds \\ithjuvenile hormone activity and chitin synthesis inhibitors, with at least one of three N-aryldiazole compounds, in particular fipronil, to control many harmful insects belonging to very varied orders. See also US Patents Nos. 6.797,724, 6,685,954, 6,413,542, 6,096,329, each of which, together with each document cited in and on each of these patents, is hereby incorporated herein by reference, as IGRs therein and formulations therein, additionally containing one or more Ibrmamidine such as amitraz or chlordimeform may be used in the practice of this invention. IGR compounds are another class of insecticides or acaricides, which are provided for in the bait formulations in this invention. Compounds belonging to this group are well known to the practitioner and represent a wide range-of different chemical classes. These compounds all act by interfering with the development or growth of the insect pests. Compounds with an ovicidal and/or larvicidal effect on the immature stages of various ectoparasites are already known, for example from U.S. Patent No. 5,439,924. Among these compounds described are those IGR compounds which act either by blocking the development of the immature stages (eggs and larvae) into adult stages, or by inhibiting the synthesis of chitin. Insect growth regulators are described, for example, in U.S. Patent 3.748.356; U.S. Patent 3,818,047: U.S. Patent 4,225.598; U.S. Patent 4.798,837; and U.S. Patent 4.751.225, as well as in HP 179,022 or U.K. 2.140,010. French Patent No. A-2.713,889 generally describes an IGR combination comprising at least one compound with juvenile hormone activity and chilin synthesis inhibitors, with at least one of three N- urylpyrazole compounds, in particular fipronil. to control many harmful insects belonging to \LT_V varied orders. rixamples of 1GR compounds uhich may be used in this invention include compounds \shich mimic juvenile hormones, in particular: azadirchtin (Agridyne) diolcnolan (Novartis) fenoxycarb (Novartis) hydroprene (Novartis) kinoprene (Novartis) methoprene (Novartis) pyriproxyten (Sumitomo/Mgk) tetrahydroazadirachtin (Agridyne) 4-chloro-2-(2-chloro-2-methylpropyl)-5-(6-iodo-3- pyridylmethoxy)pyridizin-3(2H)-one and chitin-synthesis inhibitors, in particular: chlorfluazuron (Ishihara Sangyo) cyromazine (Novartis) difliibenzuron (Solvay Duphar) flua/uron (Novartis) flucycloxuron (Solvay Duphar) flulenoxuron (Cyanamid) hexaflumuron (Dow Blanco) lufenuron (Novartis) tebufenozide (Rohm & Haas) teflubenzuron (Cyanamid) irillumuron (Bayer). These compounds are defined by their international common name (The Pesticide Manual. I01'1 edition. 1994, Ed. Clive Toinlin. Great Britain). Chitin-synthesis inhibitors also include compounds such as l-(2.6-difluorobenzoyl)-3- (2-tluoro-4-((tritluoromethyI)) phenylurea, l-(2,6-difluorobenzoyl)-3-(2-tliioro-4-(I.1.2,2- tetrafluoroethoxy))phenylurea and l-(2.6-difluorobenzoyl)-3-(2-fluoro-4-trifluoro- methyOphenylurea. Novaluron (Isagro. Italian company) is also an example of an IGR compound. Preferred IGR compounds include methoprenes, pyriproxyfens, hydroprene, cyromazine, lufenuron, l-(2,6-difluorobenzoyl)-3-(2-fluoro-4-(trifluoromethyl)phenylurea and novaluron. Other class compounds which maybe combined with the inventive ectoparasitical combination include avermectin and milbemycin derivatives, pyrethroids, benzamidazoles and imidazoles. Preferred avermectins or milbemycins include doramectin, enamectin, abamectin, eprinomectin, ivermectin, selamectin, moxidectin and milbemycin oxime. Preferred pyrethroids include the pyrethrins, permethrin, resmethrin and sumithrin. Preferred benzimidazoles include albendazole, fenbenazole, mebendazole. oxibendazole and triclabendazole. A preferred imidazoleothiazole is levamisole. The amount of these compounds to be included with the inventive ectoparasitical combination depends on the type of animal and the degree of infestation. The amounts of these compounds are easily determined by one skilled in the an. Representative amounts include O.OOlmg/kg to lOOmg/kg, with the avermectins having preferred range of 0.001 mg/kg to lOmg/kg and the other classes from 0.1 mg/kg to 100 mg/kg. Administration of the inventive formulation may be intermittent in time and may be administered daily, weekly, biweekly, monthly, bimonthly, quarterly, or even for longer durations of time. The time period between treatments depends upon factors such as the parasite(s) being treated, the degree of infestation, the type of animal, mammal or bird, and the environment where it resides. It is well within the skill level of the practitioner to determine a specific administration period for a particular situation. This invention contemplates a method for permanently combating a parasite in an environment in which the animal is subjected to strong parasitic pressure where the administration is at a frequency far below a daily administration in this case. For example, it is preferable for the treatment according to the invention to be carried out monthly on mammals, such as on dogs and on cats. Spot-on formulations may be prepared by dissolving the active ingredients into the pharmaceutically or veterinary acceptable vehicle. Alternatively, the spot-on formulation can be prepared by encapsulation of the active ingredient to leave a residue of the therapeutic agent on the surface of the animal. These formulations will vary with regard to the weight of the therapeutic agent in the combination depending on the species of host animal to be treated, the severity and type of infection and the body weight of the host. The compounds may be administered continuously, particularly for prophylaxis, by known methods. Generally, a dose of from about 0.001 to about 10 mg per kg of body weight given as a single dose or in divided doses for a period of from 1 to 5 days will be satisfactory but, of course, there can be instance where higher or lower dosage ranges are indicated and such are within the scope of this specific administration period for a particular situation. This invention contemplates a method for combating mosquitoes in an environment in which the animal is subjected to strong mosquito pressure where the administration is at a frequency far below a daily administration in this case. For example, it is preferable for the treatment according to the invention to be carried out monthly on dogs and on cats and or birds. Spot-on and pour-on formulations may be prepared by dissolving the active ingredients into the pharmaceutically or veterinary acceptable vehicle. Alternatively, the spot-on formulation can be prepared by encapsulation of the active ingredient to leave a residue of the therapeutic agent on the surface of the animal. These formulations will vary \\ith regard to the weight of the therapeutic agent in the combination depending on the species of host animal to be treated, the severity and type of infection and the body weight of the host. The compounds may be administered continuously, particularly for prophylaxis, by known methods. Generally, a dose of from about 0.001 to about 100 ing per kg of body weight of l-N-arylpyrazole and 0.01 to about 100 mg/kg of amitraz given as a single dose or in divided doses for a period of from 1 to 5 days will be satisfactory but, of course, there can be instance where higher or lower dosage ranges are indicated and such are within the scope of this invention. It is well within the routine skill of the practitioner to determine a particular dosing regimen for a specific host and parasite. Preferably, a single formulation containing the l-N-arylpyrazole derivative is in a substantially liquid carrier and is in a form which makes possible a single application or an application repeated a small number of times. The formulation will be administered to the animal over a highly localized region of the animal, preferably between the two shoulders. It is well within the routine skill of the practitioner to determine a particular dosing regimen for a specific host and parasite. Most preferably, this localized region has a surface area of less than 10 cm2, especially between 5 and 10 cm2 area. Remarkably, it has been discovered that such a formulation is highly effective against both the targeted parasites. The treatment is preferably carried out so as to administer to the host, on a single occasion, a dose containing between about 0.001 and about 100 mg/kg of a compound of formula (11). The amount of compounds of l-N-aylpyrazole for animals which are small in size is preferably greater than about 0.01 mg and in a particularly preferred way between about 1 and about 50 mg/kg of weight of animal. It also may be preferable to use controlled-release formulations. This invention also provides for a method for cleaning the coats and the skin of animals by removal of the parasites which are present and of their waste and excreta. The animals treated thus exhibit a coat which is more pleasing to the eye and more pleasant to the touch. The invention also relates to such a method with a therapeutic aim intended for the treatment and prevention of parasitoses having pathogenic consequences. In another preferred embodiment this provides for a composition for combating fleas in small mammals, in particular dogs and cats, characterized in that it contains at least one of formula (II) as defined above. The formulations of the present invention provide for the topical administration of a concentrated solution, suspension, microemulsion or emulsion for intermittent application to a spot on the animal, generally between the two shoulders (solution of spot-on type). It has been discovered that the inventive formulations are especially active against parasites when the formulations are applied to animals, such as mammals, especially dogs, cats, sheep, pigs, cattle and horses and birds, especially chickens, turkeys and quails. The ectoparasitical combination can advantageously be present in this formulation in a proportion of about 1 to about 20%, preferably of about 5 to about 15% (percentages as weight by volume = W/V). The liquid carrier vehicle comprises a pharmaceutically or veterinary acceptable organic solvent and optionally an organic cosolvent. Also contemplated are the phannaceutically or veterinary acceptable acid or base salts, where applicable, of the active compounds provided for herein. The term "acid" contemplates all pharmaceutical!) or veterinary acceptable inorganic or organic acids. Inorganic acids include mineral acids such as hydrohalic acids, such as hydrobromic and hydrochloric acids, sulfuric acids, phosphoric acids and nitric acids. Organic acids include all pharmaceutically or veterinary acceptable aliphatic, alicyclic and aromatic carboxylic acids, dicarboxylic acids tricarboxylic acids and fatty acids. Preferred acids are straight chain or branched, saturated or unsaturated C|-C':n aliphatic carboxylic acids, which are optionally substituted by halogen or by hydroxvl groups, or C6-C|? aromatic carboxylic acids. Examples of such acids are carbonic acid, formic acid, fumaric acid, acetic acid, propionic acid, isopropionic acid, valeric acid, a-hydroxy acids, such as glycolic acid and lactic acid, chloroacetic acid, benzoic acid, methane sulfonic acid, and salicylic acid. Examples of dicarboxylic acids include oxalic acid, malic acid, succinic acid, tartaric acid and maleic acid. An example of a tricarboxylic acid is citric acid. Fatty acids include all pharmaceutically or veterinary acceptable saturated or unsaturated aliphatic or aromatic carboxylic acids having 4 to 24 carbon atoms. Examples include butyric acid, isobutyric acid, sec-butyric acid, lauric acid, palmitic acid, stearic acid, oleic acid, linoleic acid, linolenic acid, and phenylsteric acid. Other acids include gluconic acid, glycoheptonic acid and lactobionic acid. The term "base" contemplates all pharmaceutically or veterinary acceptable inorganic or organic bases. Such bases include, for example, the alkali metal and alkaline earth metal salts, such as the lithium, sodium, potassium, magnesium or calcium salts. Organic bases include the common hydrocarbyl and helerocyclic amine salts, which include, for example, the morpholine and piperidine salts. The organic solvent for the liquid carrier vehicle will preferably have a dielectric constant of between about 10 and about 35, preferably between about 20 and about 30, the content of this solvent in the overall composition preferably representing the remainder to 100% of the composition. It is well within the skill level of the practitioner to select a suitable solvent on the basis of these parameters. The organic cosolvent for the liquid carrier vehicle will preferably have a boiling point of less than about 100°C, preferably of less than about 80°C, and will have a dielectric constant of between about 10 and about 40. preferably between about 20 and about 30; this cosolvent can advantageously be present in the composition according to a weight/weight (W/W) ratio with respect to the solvent of between about 1/15 and about 1/2; the cosolvent is volatile in order to act in particular as drying promoter and is miscible with water and/or with the solvent. Again, it is well within the skill level of the practitioner to select a suitable solvent on the basis of these parameters. The organic solvent for the liquid carrier includes the commonly acceptable organic solvents known in the formulation art. These solvents may be found, for example, in Remington Pharmaceutical Science, I61'1 Edition (1986). These solvents include, for example, acetone, ethyl acetate, methanol, ethanol, isopropanol, dimethylformamide, dichloromethane or diethylene glycol monoethyl ether (Transcutol). These solvents can be supplemented by various excipients according to the nature of the desired phases, such as CV Cio caprylic/capric triglyceride (Estasan or Miglyol 812), oleic acid or propylene glycol. The liquid carrier may also comprise a microemulsion. Microemulsions are also well suited as the liquid carrier vehicle. Microemulsions are quaternary systems comprising an aqueous phase, an oily phase, a surfactant and a cosurfactant. They are translucent and isotropic liquids. Microemulsions are composed of stable dispersions of microdroplets of the aqueous phase in the oily phase or conversely of microdroplets of the oily phase in the aqueous phase. The size of these microdroplets is less than 200 nm (1000 to 100,000 nm for emulsions). The interracial film is composed of an alternation of surface-active (SA) and co-surface-active (C'o-SA) molecules which, by lowering the interfacial tension, allows the microemtilsion to be formed spontaneously. The oily phase can in particular be formed from mineral or vegetable oils, from unsaturated polyglycosylated glycerides or from triglycerides, or alternatively from mixtures of such compounds. The oily phase preferably comprises triglycerides and more preferably medium-chain triglycerides, for example CVC|0 caprylic/capric triglyceride. The oily phase will represent, in particular, from about 2 to about 15%, more particularly from about 7 to about 10%, preferably from about 8 to about 9%, V/V of the microemulsion. The aqueous phase includes, for example water or glycol derivatives, such as propylene glycol, glycol ethers, polyethylene glycols or glycerol. Propylene glycol, diethylene glycol monoethyl ether and dipropylene glycol monoethyl ether are especially preferred. Generally, the aqueous phase will represent a proportion from about 1 to about 4% V/V in the microemulsion. Surfactants for the microemulsion include diethylene glycol monoethyl ether, dipropyelene glycol monomethyl ether, polyglycolysed Cx-Cm glycerides or polyglyceryl-6 dioleate. In addition to these surfactants, the cosurfactants include short-chain alcohols, such as ethanol and propanol. Some compounds are common to the three components discussed above, i.e., aqueous phase, surfactant and cosurfactant. However, it is well within the skill level of the practitioner to use different compounds for each component of the same formulation. The cosurfactant to surfactant ratio will preferably be from about 1/7 to about 1/2. There will preferably be from about 25 to about 75% V/V of surfactant and from about 10 to about 55% V/V of cosurfactant in the microemulsion.Likewise, the co-solvents are also well known to a practitioner in the formulation art. Preferred co-solvents are those which is a promoter of drying and include, for example, absolute ethanol. isopropanol (2-propanol) or methanol. The crystallization inhibitor can in particular be present in a proportion of about I to about 20% (W/V), preferably of about 5 to about 15%. The inhibitor preferably corresponds to the test in which 0.3 ml of a solution comprising 10% (W/V) of the compound of formula (I) in the liquid carrier and 10% of the inhibitor are deposited on a glass slide at 20°C and allowed to stand for 24 hours. The slide is then observed with the naked eye. Acceptable inhibitors are those whose addition provides for few or no crystals, and in particular less than 10 crystals, preferably 0 crystals. Although this is not preferred, the formulation can optionally comprise water, in particular in a proportion of 0 to about 30% (volume by volume V/V), in particular of 0 to about 5%. The formulation can also comprise an antioxidizing agent intended to inhibit oxidation in air, this agent being in particular present in a proportion of about 0.005 to about 1% (W/V), preferably of about 0.01 to about 0.05%. Crystallization inhibitors which can be used in the invention include: - polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and of vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol or polyoxyethylenated esters of sorbitan; lecithin or sodium carboxymethylcellulose; or acrylic derivatives, such as methacrylates and others, anionic surfactants, such as alkaline stearates, in particular sodium, potassium or ammonium stearate: calcium stearate or triethanolamine stearate; sodium abietate: alkyl sulphates, in particular sodium lauryl sulphate and sodium cetyl sulphate; sodium dodecylbenzenesulphonate or sodium dioctyl sulphosuccinate: or fatty acids, in particular those derived from coconut oil. - cationic surfactants, such as water-soluble quaternary ammonium salts of formula N"R'R"R'"R""Y~, in which the R radicals are identical or different optionally hydroxylated hydrocarbon radicals and Y~ is an anion of a strong acid, such as hatide, sulphate and sulphonate anions; cetyltrimethylammonium bromide is one of the cationic surfactants which can be used, - amine salts of formula N+R'R"R'", in which the R radicals are identical or different optionally hydroxylated hydrocarbon radicals; octadecylamine hydrochloride is one of the cationic surfactants which can be used, non-ionic surfactants, such as optionally polyoxyethylenated esters of sorbitan, in particular Polysorbate 80, or polyoxyethylenated alkyl ethers; polyethylene glycol stearate, polyoxyethylenated derivatives of castor oil, polyglycerol esters, polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids or copolymers of ethylene oxide and of propylene oxide, - amphoteric surfactants, such as substituted lauryi compounds of betaine. - or preferably a mixture of at least two of the compounds listed above. In a particularly preferred embodiment, a crystallization inhibitor pair will be used. Such pairs include, for example, the combination of a film-forming agent of polymeric type and of a surface-active agent. These agents will be selected in particular from the compounds mentioned above as crystallization inhibitor. Particularly preferred film-forming agents of polymeric type include: - the various grades of polyvinylpyrrolidone, - polyvinyl alcohols, and - copolymers of vinyl aceune and of vinylpyrrolidone.Especially preferred surface-active agents, include those made of non-ionic surfactants, preferably polyoxyethylenaied esters of sorbitan and in particular the various grades of polysorbate, for example Polysorbate 80. The film-forming agent and the surface-active agent can in particular be incorporated in similar or identical amounts within the limit of the total amounts of crystallization inhibitor mentioned elsewhere. The pair thus constituted secures, in a noteworthy way, the objectives of absence of crystallization on the coat and of maintenance of the cosmetic appearance of the fur, that is to say without a tendency towards sticking or towards a sticky appearance, despite the high concentration of active material. Particularly preferred antioxidizing agents are those conventional in the art and include, for example, butylated hydroxyanisole, butylated hydroxytoluene, ascorbic acid, sodium metabisulphite, propyl gallate, sodium thiosulphate or a mixture of not more than two of them. The formulation adjuvants discussed above are well known to the practitioner in this art and may be obtained commercially or through known techniques. These concentrated compositions are generally prepared by simple mixing of the constituents as defined above: advantageously, the starting point is to mix the active material in the main solvent and then the other ingredients or adjuvants are added. The volume applied can be of the order of about 0.3 to about I ml, preferably of the order of about 0.5 ml, for cats and of the order of about 0.3 to about 5 ml for dogs, depending on the weight of the animal. The pour-on solutions according to the invention, which are advantageously oily, generally comprise a diluent or vehicle and also a solvent (organic solvent) for the compound of formula (II) if the latter is not soluble in the diluent. Low concentrations of from about 0.05 to about 10% weight/volume, more particularly from about O.I to about 2%. are preferred. Optimally, the value is between about 0.25 and about 1.5%. in particular in the region of about 1%. Organic solvents which can be used in the inventive pour-on solutions, mention may be made in particular of: acetyltributvl citrate, fatty acid esters such as the dimethyl ester, diisobutyl adipate, acetone, acetonitrile, benzyl alcohol, butyl diglycol, dimethytacetamide, dimethylformamide, dipropylene glycol n-butyl ether, ethanol, isopropanol, methanol, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, monomethylacetamide, dipropylene glycol monomethyl ether, liquid polyoxyethylene glycols, propylene glycol, 2-pyrrolidone, in particular N-methylpyrroIidone, diethylene glycoi monoethyl ether, ethylene glycol and diethyl phthalate, or a mixture of at least two of these solvents. As vehicle or diluent for the inventive pour-on solutions, mention may be made in particular of: plant oils such as soybean oil, groundnut oil, castor oil, corn oil. cotton oil, olive oil, grape seed oil, sunflower oil, etc.; mineral oils such as petrolatum, paraffin, silicone, etc.; aliphatic or cyclic hydrocarbons or alternatively, for example, medium-chain (C8 to C12 in particular) triglycerides. An emollient and/or spreading and/or film-forming agent will preferably be added, this agent being selected in particular from: polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol, polyoxyethylenated sorbitan esters; lecithin, sodium carboxymethylcellulose. silicone oils, polydiorganosiloxane oils, in particular polydimethylsiloxane (PDMS) oils, for example those containing silanol functionalities, or a 45V2 oil,anionic surfactants such as alkaline stearates, in particular sodium, potassium or ammonium stearates: calcium stearate. triethanolamine stearate: sodium abietate: alkyl sulphates, in particular sodium lauryl sulphate and sodium cetyl sulphate; sodium dodecylbenzenesulphonate, sodium dioctylsulphosuccinate; fatty acids, in particular those derived from coconut oil, cationic surfactants such as water-soluble quaternary ammonium salts of formula NTR'R"R'"R"", Y- in which the radicals R are optionally hydroxylated hydrocarbon radicals and Y is an anion of a strong acid such as the halide, sulphate and sulphonate anions; cetyltrimethylamnionium bromide is among the cationic surfactants which can be used, amine salts of formula N+R'R"R'" in which the radicals R are optionally hydroxylated hydrocarbon radicals; octadecylamine hydrochloride is among the cationic surfactants which can be used, nonionic surfactants such as sorbilan esters, which are optionally polyoxyethylenated, in particular polysorbate 80, polyoxyethylenated alkyl ethers; polyoxypropylated fatty alcohols such as polyoxypropylene-styrol ether; polyethylene glycol stearate, polyoxyethylenated derivatives of castor oil, polyglycerol esters, polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids, copolymers of ethylene oxide and propylene oxide, amphoteric surfactants such as the substituted lauryl compounds of betaine; or a mixture of at least two of these agents. The solvent will be used in proportion with the concentration of the compound II and its solubility in this solvent. The emollient is preferably used in a proportion of from about 0.1 to about 10%, in particular from about 0.25 to about 5%. by volume. This invention further provides for parasitical spray formulations which comprise: a) an effective amount of an ectoparasitical combination comprising I-N- arylpyrazole derivative and amitraz; and b) a pharmaceutical or veterinary acceptable liquid carrier vehicle. Preferred carrier vehicles include isopropanol, ethanol, methanol, acetone, ether(s), propylene glycol. polyethylene glycol, glycol formal, DGME and DMSO. Examples: The following non-limiting examples illustrate the invention: Example I The following formulation according to the present invention was prepared by conventional techniques: Ingredient Amount (% w/v) fipronil 10.0 amitraz 5.0 ethanol 10.0 polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02 butylated hydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100 Example 2 The following formulation according to the present invention was prepared by conventional techniques: Ingredient Amount (% w/v) fipronil 10.0 amitraz 15.0 ethanol 10.0 polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02 butylated hydroxytoluene 0.01 diethyleneglycol monoeth) I ether QS 100 Example 3 The following formulation according to the present invention was prepared by conventional techniques: Ingredient Amount (% w/v) fipronil 10.0 amitraz 12.0 ethanol 10.0 polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02 butylated hydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100 Comparative Example 4 The following formulation not according to the present invention was prepared by conventional techniques: Ingredient Amount (% w/v) fipronil 10.0 ethanol 10.0 polyvidone 5.0 polysorbate 80 5.0 butylated hydroxyanisole 0.02 butylated hydroxytoluene 0.01 diethyleneglycol monoethyl ether QS 100 Example 5 The duration of the efficacy of the formulation of Example 3 (according to the present invention) was compared with the formulation of Comparative Example 4 against ticks on dogs. The results are presented below: Duration of Efficacy against Rhipicephalus sunguineus ticks on dogs. (% efficacy at 48-hour counts)(Table Removed)As can be seen the formulation according to the present invention remained effective for a Far longer period than fipronil alone. Example 6 The speed of the efficacy of the formulation of Example 3 (according to the present invention) was compared with the formulation of Comparative Example 4 against ticks on dogs. The results are presented below: Speed of efficacy against Rhipicephalus .sanguineus ticks on dogs. (Efficacy counts were performed 6 hours alter each weekly infestation) (Table Removed)As can be seen the formulation according to the present invention exhibit a faster rate of efficacy than a formulation comprising fipronil alone. Example 7 The duration of the efficacy of the formulation of Example 3 (according to the present invention) was compared with the formulation of Comparative Example 4 against fleas on dogs. The results are presented below: Duration of efficacy against fleas (% efficacy against fleas measured 24 hours after each weekly infestation) (Table Removed) As can be seen the formulation according to the present invention remained effective for a far longer period of time than a formulation comprising fipronil alone. This enhanced efficacy is surprising since amitraz is not known in the art to be used in treating flea infestations on mammals and birds. The above description is intended to be illustrative and not limiting. Various changes or modifications in the embodiments described herein may occur to those skilled in the art. These changes can be made without departing from the scope or spirit of the invention. We Claim: 1. A parasiticidal spot-on formulation for the treatment or prevention of parasite infestations in non-human mammals or birds, which comprises: a) an ectoparasiticidal combination comprising of 5-15% (w/v) of fipronil and 5-15% (wA/) of amitraz; b) a pharmaceutical or veterinary acceptable liquid carrier vehicle for applying the formulation to a localized region on an animal comprising a solvent and optionally a cosolvent; wherein the solvent represents the remainder to 100% of the W composition and is selected from the group consisting of benzyl alcohol, butyl diglycol, dipropylene glycol n-butyl ether, liquid polyoxyethylene glycols, propylene glycol, and diethylene glycol monoethyl ether, or a mixture thereof, and the cosolvent is selected from the group consisting of ethanol, isopropanol and methanol; wherein if the cosolvent is present, it is in a weight/weight (W/W) ratio with respect to the solvent of between 1/15 and 1/2; and c) optionally, 1 to 20% of a crystallization inhibitor selected from the group consisting of an anionic surfactant, a cationic surfactant, a non-ionic surfactant, an amine salt, an amphoteric surfactant or polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol, polyoxyethylenated sorbitan esters, lecithin, sodium carboxymethylcellulose, and acrylic derivatives, and a mixture of these 9 crystallization inhibitors. 2. The parasiticidal spot-on formulation as claimed in claim 1, wherein the said formulation optionally contains an antioxidant and/or an insect growth regulator. 3. The parasiticidal spot-on formulation as claimed in claim 2, wherein the antioxidant is selected from the group consisting of butylated hydroxyanisole, butylated hydroxytoluene, ascorbic acid, sodium metabisulphite, propyl gallate and sodium thiosuphate and/or the insect growth regulator is selected from the group consisting of azadirchtin, diofenolan, fenoxycarb, hydroprene, kinoprene, 61 methoprene, pyriproxyfen, tetrahydroazadirachtin and 4-chloro-2-(2-chloro-2- methylpropyl)-5-(6-iodo-3-pyridylmethoxy)pyridizin-3-(2H)-one. 4. The parasiticidal spot-on formulation as claimed in any one of claims 1 to 3, wherein water is present in a proportion of from 0 to 30% v/v. 5. The parasiticidal spot-on formulation as claimed in claim 1, wherein the anionic surfactant is alkaline stearates, sodium abietate; alkyl sulphates; sodium dodecylbenzenesulphonate, sodium dioctylsulphosuccinate, and fatty acids; W - the cationic surfactant is water-soluble quaternary ammonium salts of formula N*R'R"R' "R" " Y~ in which the radicals R independently are hydrocarbon radicals, optionally hydroxylated, and Y~ is an anion of a strong acid; the amine salt is an amine salt of N*R'R"R' " in which the radicals R independently are optionally hydroxylated hydrocarbon radicals; the non-ionic surfactant is optionally polyoxyethylenated sorbitan esters, polyoxyethylenated alkyl ethers, polyethylene glycol stearate, polyoxyethylenated derivatives of castor oil, polyglycerol esters, polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids, copolymers of ethylene oxide and propylene oxide; and the amphoteric surfactant is lauryl-substituted betaine compounds. W 6. The parasiticidal spot-on formulation as claimed in claim 3, wherein the pharmaceutically or veterinary acceptable carrier preferably comprises diethyleneglycol monoethyl ether, the crystallization inhibitor preferably comprises polyvinylpyrrolidone, the surfactant is preferably comprises-polysorbate 80 and the antioxidant preferably comprises butylated hydroxyanisole and butylated hydroxytoluene. 7. The parasiticidal spot-on formulation as claimed in any one of claims 1 to 3, wherein the formulation optionally contains a milbemycin or avermectin derivative, an imidazothiazide anthelmintic, a benzimidazole anthelmintic, or a pyrethroid. 62 8. The parasiticjdal spot-on formulation as claimed in claim 1, wherein the formulation preferably comprises 5-15% (w/v) of fipronil; 5-15% Amritraz; and 5-15% (w/v) of a crystallization inhibitor in the liquid earner. 9. A parasiticidal spot-on formulation as claimed in claim 1, wherein the said formulation preferably comprises a) about 10% (w/v) fipronil; b) about 12% (w/v) amitraz; 9 c) a pharmaceutical or veterinary acceptable liquid can-ier vehicle for applying the formulation to a localized region on an animal comprising a solvent and a cosolvent; wherein the solvent used is diethyleneglycol monoethyl ether.and the cosolvent used is..ethanol; and d) 10% (w/v) of a crystallization inhibitor, wherein crystallization inhibitor used is a combination of polyvinylpyrrolidone and polysorbate 80. 10. A parasiticidal spot-on formulation as claimed in claim 1, wherein the said formulation preferably comprises a) about 10% (w/v) fipronil; b) about 15% (w/v) amitraz; c) a pharmaceutical or veterinary acceptable liquid carrier vehicle for f P applying the formulation to a localized region on an animal comprising a solvent and a cosolvent; wherein the solvent used is diethyleneglycol monoethyl ether and the cosolvent used is.ethanol; and d) 10% (w/v) of a crystallization inhibitor, wherein crystallization inhibitor used is.a combination of polyvinylpyrrolidone and polysorbate 80. 11. The parasiticidal spot-on formulation as claimed in claim 1, a crystallization inhibitor is preferably, crystallization inhibitor system comprising a polymeric filmforming agent and a surfactant. 63 12. The parasiticidal spot-on formulation as claimed in claim 11, wherein the polymeric film-forming agent is polyvinylpyrrolidone, a polyvinyl alcohol, or a copolymer of vinyl acetate and vinylpyrrolidone and the surfactant is a non-ionic surfactant. 13. A medicament as and when used for the preventing, controlling, or eliminating parasites in a non-human mammal or bird, prepared using the formulation of claim 1. Dated this 22"" day of June 2006 ^X • rw^ Samita Kapoor SN/PA-1114 Agent for the Applicant 64 I

Documents:

3619-delnp-2006-Abstract-(03-01-2012).pdf

3619-delnp-2006-abstract.pdf

3619-delnp-2006-Claims-(03-01-2012).pdf

3619-delnp-2006-Claims-(06-08-2013).pdf

3619-DELNP-2006-Claims-(09-05-2012).pdf

3619-delnp-2006-claims.pdf

3619-delnp-2006-Correspodence Others-(03-01-2012).pdf

3619-DELNP-2006-Correspodence Others-(09-01-2012).pdf

3619-DELNP-2006-Correspondence Others-(01-07-2011).pdf

3619-DELNP-2006-Correspondence Others-(09-05-2012).pdf

3619-DELNP-2006-Correspondence Others-(16-01-2012).pdf

3619-DELNP-2006-Correspondence Others-(30-03-2011).pdf

3619-DELNP-2006-Correspondence Others-(30-06-2011).pdf

3619-delnp-2006-Correspondence-Others-(06-08-2013).pdf

3619-delnp-2006-Correspondence-Others-(26-07-2013).pdf

3619-delnp-2006-correspondence-others-1.pdf

3619-delnp-2006-correspondence-others.pdf

3619-delnp-2006-description (complete).pdf

3619-delnp-2006-Form-1-(03-01-2012).pdf

3619-delnp-2006-form-1.pdf

3619-delnp-2006-form-18.pdf

3619-delnp-2006-Form-2-(03-01-2012).pdf

3619-delnp-2006-form-2.pdf

3619-delnp-2006-form-26.pdf

3619-DELNP-2006-Form-3-(01-07-2011).pdf

3619-DELNP-2006-Form-3-(09-05-2012).pdf

3619-DELNP-2006-Form-3-(30-06-2011).pdf

3619-delnp-2006-form-3.pdf

3619-delnp-2006-form-5.pdf

3619-DELNP-2006-GPA-(09-01-2012).pdf

3619-DELNP-2006-GPA-(16-01-2012).pdf

3619-DELNP-2006-Petition-137-(09-05-2012).pdf