Label: SENSODYNE PRONAMEL CLINICAL ENAMEL STRENGTH FRESH BREATH- potassium nitrate, sodium fluoride paste, dentifrice
- NDC Code(s): 0135-7753-01
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 1, 2025
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- Active ingredients
- Purposes
- Uses
- Warnings
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Directions
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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. Minimize swallowing.
- children under 12 years of age:Consult a dentist or doctor.
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adults and children 12 years of age and older:
- Other information
- Inactive ingredients
- Questions or comments?
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Additional Information
ALWAYS FOLOW THE LABEL
SENSODYNE PRONAMEL CLINICAL ENAMEL STRENGTH
CLINICALLY PROVEN ENAMEL STRENGTHENING
REPAIRS
66%of enamel microdamage in the most vulnerable areas of your teeth^
24/7 PROTECTION
against early stage cavities, sensitivity and future enamel damage**
To help protect teeth for life**
LEAVES YOUR MOUTH
feeling clean and fresh
FRESH MINT
*Vs. your mouth’s natural defenses.
**With twice daily brushing.
^Acid weakened enamel. On average as shown in 7 day lab test.
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INGREDIENTS AND APPEARANCE
SENSODYNE PRONAMEL CLINICAL ENAMEL STRENGTH FRESH BREATH
potassium nitrate, sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-7753 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) SODIUM FLUORIDE 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) SODIUM LACTATE (UNII: TU7HW0W0QT) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) XANTHAN GUM (UNII: TTV12P4NEE) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SACCHARIN SODIUM (UNII: SB8ZUX40TY) METHYL VINYL ETHER AND MALEIC ACID COPOLYMER (1750000 WAMW) (UNII: 9F20VSM0VU) SODIUM HYDROXIDE (UNII: 55X04QC32I) Product Characteristics Color white Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-7753-01 1 in 1 CARTON 12/01/2025 1 96.4 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 M021 12/01/2025 Labeler - Haleon US Holdings LLC (079944263)

