Label: MADE BY DENTISTS SENSITIVE AND WHITENING FRESH MINT- potassium nitrate, sodium fluoride paste
- NDC Code(s): 75065-029-06
- Packager: MADE BY DENTISTS INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 27, 2024
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- Drug Facts
- Active ingredient:
- 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?
- Label
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INGREDIENTS AND APPEARANCE
MADE BY DENTISTS SENSITIVE AND WHITENING FRESH MINT
potassium nitrate, sodium fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75065-029 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 WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) XYLITOL (UNII: VCQ006KQ1E) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SACCHARIN SODIUM (UNII: SB8ZUX40TY) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) HYDROGEN PEROXIDE (UNII: BBX060AN9V) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75065-029-06 1 in 1 CARTON 02/22/2024 1 120 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 02/22/2024 Labeler - MADE BY DENTISTS INC (117405870)