Label: MADE BY DENTISTS ENAMEL 10 FLUORIDE ANTICAVITY- potassium nitrate, sodium fluoride paste
- NDC Code(s): 75065-033-06, 75065-033-07
- Packager: Made By Dentists Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 16, 2026
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- Drug Facts
- Active ingredients :
- Use:
- Warnings:
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Directions:
- Adults and children 12 years of age and older: Apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly, for at least 1 minute twice a day, (morning and evening) or as recommended by a dentist or doctor.
- Make sure to brush all sensitive areas of the teeth.
- Children under 12 years of age: Consult a dentist or doctor.
- Inactive ingredients:
- Questions or comments?
- Package Labeling:
- Package Labeling:
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INGREDIENTS AND APPEARANCE
MADE BY DENTISTS ENAMEL 10 FLUORIDE ANTICAVITY
potassium nitrate, sodium fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75065-033 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM NITRATE (UNII: RU45X2JN0Z) (NITRATE ION - UNII:T93E9Y2844) POTASSIUM NITRATE 50 mg in 1 g SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) HYDRATED SILICA (UNII: Y6O7T4G8P9) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) XYLITOL (UNII: VCQ006KQ1E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75065-033-06 1 in 1 CARTON 08/01/2026 1 120 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:75065-033-07 1 in 1 CARTON 09/01/2026 2 20 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 08/01/2026 Labeler - Made By Dentists Inc (117405870) Registrant - Made By Dentists Inc (117405870)




