Label: SENSODYNE PRONAMEL GENTLE WHITENING ADVANCED- potassium nitrate and sodium fluoride paste
- NDC Code(s): 0135-0580-01, 0135-0580-02
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 4, 2024
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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:
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- apply at least a 1-inch strip of the product onto a soft bristle toothbrush.
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- brush teeth thoroughly for at least 1 minute twice a day (morning and evening), and not more than 3 times a day, or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Spit out after brushing.
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- children under 12 years of age: Consult a dentist or doctor.
- Other information
- Inactive ingredients
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Questions or comments?
1-866-844-2797
Additional information
ALWAYS FOLLOW THE LABEL
SENSODYNE PRONAMEL
Does not contain: SLS/sulfates • artificial dyes • parabens • triclosan • peroxide
Acidic foods and drinks can cause enamel loss that can lead to yellowing, dullness and sensitivity. Pronamel has a specialty formulation to help rebuild and restore acid weakened enamel, helping prevent enamel loss for strong, healthy teeth.
ACID ATTACKS ENAMEL
WEAKENING THE ENAMEL STRUCTURE
PRONAMEL REBUILDS & RESTORES ENAMEL
FOR STRONG HEALTHY TEETH
Healthy white teeth start with strong enamel.
Pronamel has a proven specialist technology that has been developed to maximize the effect of fluoride on enamel.
With twice-daily brushing, Pronamel helps to:
• Rebuild enamel strength for strong, healthy teeth
• Protect against the effects of dietary acids
• Relieve sensitive teeth
• Freshen breath
• Protect against cavities
Recyclable Carton Save Water
Turn off tap while brushing
Trademarks are owned by or licensed to the GSK group of companies.
©2021 GSK group of companies or its licensor.
Distributed by:
GSK Consumer Healthcare
Warren, NJ 07059
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INGREDIENTS AND APPEARANCE
SENSODYNE PRONAMEL GENTLE WHITENING ADVANCED
potassium nitrate and sodium fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0580 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 1.15 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) XANTHAN GUM (UNII: TTV12P4NEE) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SACCHARIN SODIUM (UNII: SB8ZUX40TY) 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:0135-0580-01 1 in 1 CARTON 03/15/2021 1 184 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0135-0580-02 4 in 1 CARTON 07/01/2023 2 184 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 03/15/2021 Labeler - Haleon US Holdings LLC (079944263)