Title of Invention

AN ORAL PRODUCT FOR REMINERALIZATION OF TEETH

Abstract

An oral product for remineralizing teeth comprising: (i) a first composition comprising from about 0.01 to about 30% by weight of a water-soluble calcium phosphate/or monolithic combination of water soluble calcium and phosphate salts, the composition having a pH less than 7; and (ii) a second composition including from about 0.01 to about 30% by weight of an alkaline material and an anticaries effective amount of a fluoride ion source, the second composition having a pH greater than 7.5 and stored separately from the first composition in a manner to avoid contact between the phosphate and the alkaline material.

Full Text

FORM2 THE PATENTS ACT, 1970 (39 of 1970) COMPLETE SPECIFICATION (See section 10; rule 13) 1. Title of the invention. AN ORAL PRODUCT FOR REMINERAUZATION OF TEETH 2. Applicant (a) Hindustan Lever Limited (b) 165/166, Backbay Reclamation, Mumbai 400 020 Maharashtra, India. (c) a company incorporated under the Indian Companies Act, 1913. The following specification (particularly) describes the nature of this invention (and the manner in which it is to be performed) REMINERALIZATION OF TEETH BACKGROUND OF THE INVENTION Field of the Invention The invention relates to oral compositions and methods employing such compositions for the remineralization of dental enamel. The Related Art In the mouth, there is a natural equilibrium between hydroxyapatite being dissolved from the enamel of teeth and hydroxyapatite being formed on or in the teeth from substances occurring naturally in the saliva. This equilibrium is shifting continuously. Among other factors, it is determined by diet and physical condition. If the equilibrium is such that hydroxyapatite is dissolved, a cariogenic condition arises which is referred to as demineralization. If the equilibrium is such that hydroxyapatite is being formed in demineralized enamel, this is referred to as remineralization. By remineralization, pre-existing tooth decay and caries can be reduced or eliminated by natural means. It has long been known that fluoride-providing compounds, even in low concentrations, promote the remineralization process. They thereby reduce pre-existing carious conditions in the tooth structure. Fluoride is 2 most effective during the developmental years from childhood to young adulthood. Improved remedies are necessary, especially beyond the formative years. Attempts have been made to arrest or prevent progression of caries by incorporation, of calcium and phosphate ions through dietary and dentifrice means. A significant hurdle to this approach has been maintaining the calcium and phosphate ions available in a non-precipitated form Two phase or separately compartmented calcium and phosphate compositions have been proposed. GB Patent 1,408,922 (Raff et al.) suggests a two-compartment tube, the first being filled with a toothpaste containing calcium chloride and the second containing disodium hydrogen phosphate. Upon dispensing, the compositions are mixed thereby causing the precipitation of calcium phosphate onto the teeth. A similar approach is reported by Tung in U.S. Patent 5,037,639 and U.S. Patent 5,268,167. The restorative compositions disclosed therein employ amorphous calcium phosphate or solutions which will form amorphous calcium phosphate suspended in a carrier. Suitable carriers were said to include gels, chewing gum, powders, mouthrinses, carbonated solutions and toothpaste. These compositions are said to have long range structure; however, they are thought to be homogeneous when measured on an Angstrom Scale. Under physiological conditions the amorphous calcium compounds have high solubilities, high formation rates and high rates of conversion to apatite. The rates of formation and conversion allow remineralization of the 3 dental tissue to occur at a greater speed. Doubts have been raised however with respect to the efficacy of such treatment. Better systems need to be developed. Accordingly, it is an object of the present invention to provide an oral product and method for building stronger, healthier teeth. Another object of the present invention is to provide an oral product and method for remineralizing enamel which can be accomplished by a consumer without intervention of a dentist. These and other objects of the present invention will become more readily apparent through the following summary and detailed discussion. SUMMARY OF THE INVENTION An oral product is provided for remineralizing teeth which includes: (i) a first composition comprising from about 0.01 to about 30% by weight of a water-soluble calcium phosphate or monolithic combination of water soluble calcium and phosphate salts, the composition having a pH less than 7; and (ii) a second composition including from about 0.01 to about 30% by weight of an alkaline material and an anticaries effective amount of a fluoride ion source, the second 4 composition having a pH greater than 7.5 and stored separately from the first composition in a manner to avoid contact between the phosphate and the alkaline material. DETAILED DESCRIPTION OF THE INVENTION Unlike much of the previous technology, it has been found that remineralization products do not need to separate calcium from phosphate ions in a storage system prior to use Now it has been discovered that a water soluble calcium phosphate salt can be stored within one composition held at a low pH. Activation of this composition to deposit hydroxyapatite onto teeth is achieved by mixing this first composition with a second composition containing fluoride and having a high pH. Although not wishing to be bound by any theory, it is theorized that upon mixing against the teeth, the soluble calcium phosphate of the first composition interacts with fluoride of the second composition. The alkaline environment of the second composition then causes precipitation of a calcium fluoro phosphate amorphous salt. Transformation of a monocalcium salt cascades downward to the di, octa and then eventually fluoridated hydroxyapatite in the presence of the high pH. Preferably fluoride should only be in the second composition so that it co-precipitates as an element of hydroxyapatite. 5 Separate storage of the two compositions of this invention may be accomplished through a dual compartment dispenser. U.S. Patent 4,687,663 (Schaeffer) discloses a dual-compartment package respectively storing a peroxide gel and a bicarbonate paste. Pump packaging with multiple compartments is reported in U.S. Patent 5,038,963 (Pettengill et al. ) and U.S. Patent 5,020,694 (Pettengill) which are embodied in a U.S. product known as Mentadent® Baking Soda & Peroxide. Of course, delivery of compositions according to the present invention is not limited to unitary albeit multicompartmented dispensers nor to totally segregated compartments. The dispenser may be a system in the form of two individual tubes quite separate from one another but packaged within a kit. Ribbons of the dentifrice from each tube are delivered to a toothbrush with mixing of the compositions occurring in the mouth. Delivery may also be from a single chambered tube except that each of the two compositions are semi solid strips positioned side-by-side "touching but not mixing with one another. The relatively high viscosity of the products prevents any substantial transference of either pH change or components between the two strips. Illustrative of this technology is a U.S. product sold by Colgate® under the Baking Soda & Peroxide brand. Still another method of delivery may be a single composition such as a paste or gel housing an alkaline environment. Monocalcium phosphate compositions may be dispersed throughout the alkaline composition yet separated from contact by a coating encapsulating the phosphate. 6 Activation occurs in the mouth through the presence of water or saliva which penetrates the encapsulating coating releasing phosphate salt to interact with the alkaline environment. A critical component of the first composition of this invention is a water soluble calcium phosphate salt. By the term "water soluble" is meant a solubility of at least 0.1 gram in 100 ml water at 25°C. Most preferred is monocalcium hydrogen phosphate but also of potential use are calcium polyol phosphates (e.g. calcium glycerophosphate) and monocalcium ammonium phosphate salts. Monolithic compositions of water soluble calcium and phosphate salts may be employed as alternatives to pre¬formed water soluble calcium phosphates. By the term "monolithic" is meant separate water soluble calcium salts and phosphate salts which from solution may metathesize into calcium phosphates in solution or later upon mixing with the second composition. Illustrative calcium salts include the halides, sulphates, nitrates, citrates, sugars and C1-C6 carboxylates. Most preferred is calcium chloride, calcium sulphate and calcium acetate. The monolithic partner phosphate salts may be alkali, ammonium or combination salts thereof. Examples include sodium ammonium phosphate, sodium phosphate, ammonium phosphate and potassium phosphate. The water-soluble calcium phosphate salts or the monolithic calcium and phosphate salts (by weight of calcium and phosphate ions only) may be present in amounts ranging from 0.01 to 30%, preferably 7 from 0.1 to 20%, optimally from 1 to 10% by weight of the first composition. Solubility of the phosphate salt is maintained in the first composition by having an acidic environment. The pH will be less than 7, preferably from 1 to 6.5, more preferably from 1.8 to 6, optimally from 2.5 to 5.5. The second composition of the present invention requires an alkaline material so that the second composition has a pH greater than 7, preferably from 7.2 to 11, more preferably from 8 to 10, optimally from 8.5 to 9.5. Alkaline materials suitable to achieve the pH are sodium bicarbonate, potassium bicarbonate, sodium carbonate, potassium carbonate, calcium carbonate, calcium oxide, sodium hydroxide, potassium hydroxide and mixtures thereof. Amounts of the alkaline material may range from 0.1 to 60%, preferably from 0.5 to 30%, more preferably from 1 to 20%, optimally from 3 to 15% by weight of the second composition. An important further component of the second composition is a fluoride anticaries compound. Illustrative of such fluoride compounds are sodium fluoride, potassium fluoride, calcium fluoride, magnesium fluoride, stannous fluoride, stannous monofluorophosphate, sodium monofluorophosphate and copper fluoride. Most preferred is sodium fluoride. These sources should release anywhere from about 25 to about 5,000 ppm of fluoride ion. ' The anticaries compound will normally be present in an 8 amount from about 0.01 to about 5%, preferably from 0.1 to 2.5%, optimally from 0.2 to 1.5% by weight of combined first and second compositions. The compositions of the present invention may be in the form of either a toothpaste, gel, powder or mouthwash. Most preferably the compositions are either pastes or gels. Especially suitable is where the phosphate salt is incorporated in a gel and the alkaline material incorporated into a paste. These compositions may include water or be anhydrous. The phosphate salt as well as the alkaline material will be delivered through a pharmaceutically acceptable carrier. The term "pharmaceutically acceptable carrier" will include such functional ingredients as water, humectants, abrasives, thickeners, surfactants and combinations thereof. Total levels of these materials may range anywhere from about 1 to about 99%, preferably from 20 to 801, optimally from 30 to 60% by weight. Acidity in the first composition may be achieved by formulating with a peroxide such as hydrogen peroxide, inorganic acids such as phosphoric, hydrochloric, nitric or boric acids, and organic C2-C20 carboxylic acids such as citric, malic, lactic, alginic, succinic, tartaric and ascorbic acids. Soluble salts may also be employed such as potassium bitartrats, sodium acid citrate, acid phosphate and pyrophosphate salts such as monosodium phosphate and disodium pyrophosphate. Levels of the acidity inducing - 9 substances may range in amounts from about 0.1 to about 20%, preferably from about 0.5 to about 10%, optimally from 1.0 to 8% by weight of the first composition. Hydrogen peroxide and phosphoric acid are the preferred substances. Among the carriers, water when present may range in amounts from about 1 to 95%, preferably from 20 to 60%, optimally from 30 to 50% by weight of each of the compositions. Of course some formulations may be anhydrous. Humectants are usually also present as one of the carriers. Illustrative of this category are sorbitol, maltitol, mannitol, glycerin and polyethylene glycols (e.g. Carbowax). Amounts of the humectant may range from 1 to 60%, preferably from about 5 to about 50%, optimally from 10 to 40% by weight of each composition. Abrasives are normally present in toothpastes and some gels. These may include sodium metaphosphate, dicalcium phosphate (which is not considered a water-soluble phosphate), calcium pyrophosphate, silica, alumina, chalk, insoluble bicarbonate salts, and mixtures thereof. Amounts of the abrasives may range from about 1 to about 80%, preferably from 5 to 50% by weight of each composition. Thickeners are a further type of carrier which can be included in the compositions of this invention. Illustrative thickeners such as sodium carboxy- methyl cellulose, hydroxy ethyl cellulose, methyl cellulose, ethyl 10 ellulose, gum tragacanth, gum arabic, gum karaya, sodium lginate, carrageenan, guar, xanthan gum, Irish moss, tarch, modified starch, Carbomers (crosslinked acrylates) nd mixtures thereof. Inorganic substances may also be uitable, especially silica aerogels and magnesium aluminum ilicate (e.g. Veegum). Amounts of the thickener may range rom about 0.01 to about 30%, preferably from 0.1 to 20%, Optimally from 0.5 to 15% by weight of a composition. Surfactants are also considered to be within the :arrier definition. Surfactants may either be anionic, Lonionic, cationic or amphoteric. Most preferred are iodium lauryl sulphate, sodium dodecylbenzene sulphonate md sodium lauryl sarcosinate. Surfactants may be present and an amount from about 0.5 to about 10%, preferably from 1.8 to 5% by weight of a composition. Gel compositions are structured with substances than can be characterized as either humectants or surfactants. for instance, a typical gel structurant is a polyoxyethylene-polyoxypropylene copolymer such as those sold by the BASF Corporation under the trademark Pluronic® F88, F99, F108 and F127. These materials are also known as Poloxamers and employed in amounts from about 5 to about 30%, preferably between about 18 and about 25% by weight of a composition. Flavors may also be present in the compositions. These flavors may be based on oils of spearmint and peppermint. Examples of other flavoring materials include menthol, clove, wintergreen, eucalyptus and aniseed. 11 Flavors may range in concentration from about 0.1 to about 51 by weight of a composition. Sweetening agents may also be included such as saccharin, sodium cyclamate, aspartame, ace-sulfame, xylitol and combinations thereof at levels from 0.1 to 10% by weight of a composition. Gel compositions incorporating hydrogen peroxide may include a sequestering agent(s) such as a pyrophosphate or other phosphate for chelation of ferric/ferrous ion as well as other transition metal ions to enhance hydrogen peroxide stability. The sequestering agents may also be included within the paste compositions and are present in amounts from about 0.01 to about 20% by weight of a composition. Most preferred chelatants are tetrasodium pyrophosphate, sodium tripolyphosphate and sodium hexametaphosphate, all known to be effective at lower pH with little affinity for calcium ion. Other organic chelating agents such as sodium ^citrate and zinc citrate are also useful. Other additives may also be incorporated such as preservatives, silicones, other synthetic or natural polymers such as Gantrez S97®, antitartar actives and antigingivitis actives. Among the antitartar agents are included zinc citrate, tetrasodium pyrophosphate, disodium pyrophosphate, dipotassium pyrophosphate, tetrapotassium pyrophosphate and mixtures thereof. Antigingivitis actives may include thymol, Triclosan, stannous gluconate and mixtures thereof. Amounts of each of the aforementioned 12 ingredients will depend upon their function. Generally each of these substances will range in amounts from about 0.01 to about 20% by weight of a composition. Except in the operating and comparative examples, or where otherwise explicitly indicated, all numbers in this description indicating amounts of material ought to be understood as modified by the word "about". The following examples will more fully illustrate the embodiments of this invention. All parts, percentages and proportions referred to herein and in the appended claims are by weight of either the first or second composition unless otherwise indicated. EXAMPLE 1 Typical of the present invention is a first composition in the form of a gel and a second composition in the form of a paste. Each of these formulations is held in a separate compartment of a dual-compartment dispenser similar to that disclosed in U.S. Patent 5,038,963 (Pettengill et al.). Gel Composition 1A INGREDIENT WEIGHT % Glycerin 40.00 Pluronic F-127 20.00 Monocalcium Phosphate 5.00 13 Monohydrate Hydrogen Peroxide (35% Active) 4.285 Phosphoric Acid 0.650 Tetrasodium Pyrophosphate 0.50 FD&C Blue No. 1 0.01 Water Balance Paste Composition IB INGREDIENT WEIGHT % Polyol II (70% Sorbitol) 40.50 Syloid 63XX (Hydrated Silica) 15.00 Sodium Bicarbonate 10.00 Sylox 15X 6.00 Polyethylene Glycol 1450 (PEG-32) 3.00 Ethyl Alcohol 38B 2.84 Sodium Lauryl Sulphate 2.98 Flavor 1.10 Cellulose Gum 0.80 Sodium Saccharin 0.54 Menthol 0.50 Sodium Fluoride 0.44 Titanium Dioxide 0.30 Water Balance EXAMPLE 2 Another system typical of the present invention is a 'two part toothpaste. Each part is placed in a dual-compartment dispenser similar to that of Example 1. COMPONENTS PASTE 2A (% WEIGHT) PASTE 2B (% WEIGHT) Sorbitol (70% Active) 28.50 — Syloid 63XX (Hydrated Silica) 20.00 18.0 Glycerin 28.00 32.0 Monocalcium Phosphate 6.49 — 14 Citric Acid 5.00 — Syloid 244 (Thickening Silica) 3.00 0.5 Xanthan Gum 0.50 — Sodium Fluoride — 0.44 FD&C Blue No. 1 0.01 — Sodium Bicarbonate — 25.0 Sodium Lauryl Sulphate -- 1.5 Sodium Carboxymethyl Cellulose — 0.8 Flavor -- 1.0 Titanium Dioxide — 0.4 Sodium Saccharin — 0.2 Water balance balance The pH of Paste 2A is approximately 2.0. Paste 2B has a pH of approximately 9.0. Strips of each of these are extruded onto a toothbrush. These strips are then brushed against the teeth thereby mixing them together. Hydroxyapatite is formed in the mixing process and deposits onto the teeth. EXAMPLE 3 Yet another system typical of the present invention is a two part toothpaste as described below. Each part is placed in a dual-compartment dispenser similar to that of Example 1. COMPONENTS PASTE 3A (% WEIGHT) PASTE 3B (% WEIGHT) Sorbitol (70% Active) 30.50 — Alumina 20.00 18.0 Polyol II 10.00 32.0 Malic Acid 5.00 — Monocalcium Phosphate 4.50 — Syloid 244 (Thickening Silica) 3.00 0.5 Xanthan Gum 0.50 — 15 Sodium Fluoride -- 0.44 FD&C Blue No. 1 0.01 — Sodium Bicarbonate -- 25.0 Sodium Lauryl Sulphate -- 1.5 Sodium Carboxymethyl Cellulose -- 0.8 Flavor __ 1.0 Sodium Carbonate -- 0.4 Sodium Saccharin -- 0.2 Water balance balance The pH of Paste 3A and 3B respectively are approximately 2 and 9. Strips of each of these pastes are placed onto a toothbrush. These strips are then brushed against the teeth thereby mixing them together. Hydroxyapatite is formed in the mixing process and deposits on the teeth. EXAMPLE 4 This Example illustrates use of a monolithic calcium and phosphate salt combination to deliver the water soluble monocalcium phosphate component. Separate gel and paste formulations representing the first and second compositions of this invention were prepared with the following compositions. Gel Composition 4A INGREDIENT WEIGHT % Glycerin 40.00 Pluronic F-127® 20.00 _Hydrogen Peroxide (35% Active) 4.29 Calcium Chloride Dihydrate 2.10 Dibasic Sodium Phosphate 1.00 16 I Phosphoric Acid (85% Active) 1.50 Sodium Citrate 0.53 FD&C Blue No. 1 0.01 Water Balance Paste Composition 4B INGREDIENT WEIGHT % Polyol II (70% Sorbitol) 40.50 Syloid 63XX (Hydrated Silica) 15.00 Sodium Bicarbonate 10.00 Sylox 15X 6.00 Polyethylene Glycol 1450 (PEG-32) 3.00 Ethyl Alcohol 38B 2.84 Sodium Lauryl Sulphate 2.98 Flavor 1.10 Cellulose Gum 0.80 Sodium Saccharin 0.54 Menthol 0.50 Sodium Fluoride 0.44 Titanium Dioxide 0.30 Water Balance EXAMPLE 5 Yet another system typical of the present invention is a two part toothpaste as described below. Each part is placed in a dual compartment dispenser similar to that of Example 1. Gel Composition 5A INGREDIENT WEIGHT % Glycerin 40.00 Pluronic F-127 20.00 Monocalcium Phosphate Monohydrate 3.10 17 Phosphoric Acid (85% Active) 0.85 Water Balance Past Composition 5B INGREDIENT WEIGHT % Polyol II (70% Sorbitol) 46.68 Syloid 63XX (Hydrated Silica) 15.00 Sodium Carbonate 6.50 Sylox 15X (Hydrated Silica) 6.00 Polyethylene Glycol 1450 (PEG 32) 5.00 Ethyl Alcohol 38B 2.84 Sodium Lauryl Sulphate 2.98 Flavor 1.00 Cellulose Gum 0.80 Sodium Saccharin 0.50 Menthol 0.50 Sodium fluoride 0.44 Titanium Dioxide 0.30 Water Balance The pH of 5A and 5B respectively are approximately 2.7 and 9.5 EXAMPLE 6 This Example illustrates use of monocalcium phosphate in a Gel composition along with Triclosan solubilized in alcohol. Gel Composition 6A INGREDIENT WEIGHT % Glycerin 40.00 Pluronic F-127 20.00 Alcohol SDA 38B 5.00 Monocalcium Phosphate, 1.55 18 Monohydrate Phosphoric Acid (95% Active) 0.45 Hydrogen Peroxide (35% Active) 4.29 Irgacare® MP (Triclosan) 0.67 Water Balance Past Composition 6B INGREDIENT WEIGHT % Polyol II (70% Sorbitol) 46.68 Syloid 63XX (Hydrated Silica) 15.00 Sodium Bicarbonate 10.00 Sylox 15X (Hydrated Silica) 6.00 Polyethylene Glycol 1450 (PEG 32) 3.00 Ethyl Alcohol 38B 2.84 Sodium Lauryl Sulphate 2.98 Flavor 1.10 Cellulose Gum 0.80 Sodium Saccharin 0.54 Menthol 0.50 Sodium Fluoride 0.44 Titanium Dioxide 0.30 | Water | Balance The pH of 6A and 6B respectively are approximately 2.7 and 9.2 EXAMPLE 7 Another Example is shown using monocalcium phosphate in a Gel composition. Here Triclosan is incorporated into a Paste composition of elevated pH for eventual combination with the Gel. Gel Composition 7A INGREDIENT WEIGHT % Glycerin 40.00 Pluronic F-127 20.00 19 Hydrogen Peroxide (35% Active) 4.29 Monocalcium Phosphate, Monohydrate 3.10 Phosphoric Acid (95% Active) 0.85 Water Balance Paste Composition 7B INGREDIENT WEIGHT % Polyol II 38.50 Syloid 63XX (Hydrated Silica) 30.00 IPA* 15.00 Sodium Carbonate 7.00 Sylox 15X (hydrated Silica) 2.00 Ethyl Alcohol 38B 2.84 Sodium Lauryl Sulphate 2.98 Flavor 1.30 Irgacare® MP (Triclosan) 0.55 Sodium Saccharin 0.5.4 Cellulose Gum 0.80 Menthol 0.50 Sodium fluoride 0.44 Titanium Dioxide 0.30 Water Balance The pH of 6A and 6B respectively are approximately 2.7 and 9.2 EXAMPLE 8 Calcium phosphate remineralization technology according to the present invention was evaluated both through in vivo and in vitro tests. Results are presented below. A) Animal Caries Summary of Experimental Design: Sprague Dawley rats were infected with caries producing bacteria, then treated 20 with slurries of experimental products for three weeks. The animals were also fed a cariogenic diet high in sugar. At end of treatment phase, teeth were scored for caries with total enamel caries incidence being the primary anticaries efficacy variable. TOTAL ENAMEL CARIES INDICENCE - 1100 ppm F as NaF Dual phase silica base Baking Soda + Peroxide toothpaste without Fluoride. ** Dual phase silica base Baking soda + Peroxide toothpaste with 1,000 ppm Fluoride ion from NaF. *** NaF dual phase silica base Baking Soda + Peroxide toothpaste with 1,200 ppm Ca, 8,000 ppm PO4 and 1,100 ppm F ions. From the Table it is seen that the sodium fluoride formulation was significantly better for caries protection than the non-fluoride placebo. Yet even more efficient was sodium fluoride in combination with calcium and phosphate in a system according to the present invention and as embodied in Example 1. B) In Vitro Remineralization Studies Summary of Experimental Design: Human enamel specimens were prepared to have artificial caries-like lesions. The specimens had their initial surface hardness measured before initiation of the treatment phase. The 21 cyclic treatment regimen consisted of treatment, remineralization and demineralization phases over the course of 21 days. At the end of the treatment regimen, the specimen surface hardness was remeasured. The change in their Vickers Hardness Numbers (Delta VHN) indicated the degree of remineralization provided by the test products. In Vitro Remineralization (1100 ppm F as NaF) ** *** ** * * toothpaste without Fluoride. Sodium Fluoride silica base toothpaste (USP Ref. Standard with 1,100 ppm Fluoride) NaF dual phase silica base Baking Soda + Peroxide toothpaste with 1,200 ppm Ca, 8,000 ppm PO4/ 1,100 ppm Fluoride ion. NaF dual phase silica base Baking Soda + Peroxide toothpaste with 1,200 ppm Ca, 8,000 pm PO4, 1,100 ppm Fluoride ion and 6,000 ppm Zn (as 2% zinc citrate) As in the in vivo studies, sodium fluoride as expected was better than the placebo having no fluoride. Incorporation of calcium and phosphate in accordance with the present invention and as shown in the system under Example 1 significantly improved teeth hardness relative to the same system containing only sodium fluoride. An even 22 greater improvement in hardness was evidenced by the further addition of zinc citrate. In Vitro Remineralization (1500 ppm F as Sodium Monofluorophosphate) * Dual phase silica base Baking Soda + Peroxide toothpaste without Fluoride ** MFP silica base toothpaste *** MFP dual phase silica base Baking Soda + Peroxide toothpaste with 2,500 ppm Ca, 16,000 ppm PO4 and 1,500 ppm Fluoride ion. Sodium monofluorophosphate as expected was better for improving tooth hardness than a placebo without fluoride. Addition of calcium and phosphate according to the present invention significantly enhanced the activity of sodium monofluorophosphate. The foregoing description and examples illustrate selected embodiments of the present invention. In light thereof variations and modifications will be suggested to one skilled in the art, all of which are within the spirit and purview of this invention. 23 We Claim: 1. An oral product for remineralizing teeth comprising: ■ ■* (i) a first composition comprising from about 0.01 to about 30% by weight of a water-soluble calcium phosphate/or monolithic combination of water soluble calcium and phosphate salts, the composition having a pH less than 7; and (ii) a second composition including from about 0.01 to about 30% by weight of an alkaline material and an anticaries effective amount of a fluoride ion source, the second composition having a pH greater than 7.5 and stored separately from the first composition in a manner to avoid contact between the phosphate and the alkaline material. 2. The product according to claim 1 wherein the water- soluble phosphate salt is monocalcium hydrogen phosphate. 3. The product according to claim 1 wherein the alkaline material is selected from the group consisting of sodium bicarbonate, potassium bicarbonate, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, calcium carbonate, calcium oxide and mixtures thereof. 4. The product according to claim 1 wherein the pH of the first composition ranges from 2.5 to 5.5. 5. The product according to claim 1 wherein the ph of the second composition ranges from 7.2 to 11. 6. The product according to claim 1 wherein the pH of the first composition results from inclusion of a compound selected from the group consisting of hydrogen peroxide, inorganic acids, C2-C20 carboxylic acids and mixtures thereof. 24 7. The product according to claim 1 wherein the monolithic combination of water soluble calcium salts are selected from the group consisting of calcium chloride, calcium sulphate and calcium acetate and the respective phosphate salts are selected from the group consisting of sodium phosphate, ammonium phosphate and sodium ammonium phosphate. 8. The product according to claim 1 optionally comprising from about 0.01 to about 20% by weight of triclosan. 9. The product according to claim 1 optionally comprising from about 0.01 to about 20% by weight of a zinc salt. Dated this 8th day of September 2000 Siddhartha Nag of S. Majumdar & CO. Applicant's Agent 25

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