Label: SENSODYNE ADVANCED WHITENING- potassium nitrate paste
- NDC Code(s): 0135-0479-01, 0135-0479-02
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 4, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- 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), 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.
- 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 (Advanced Whitening)
- Questions or comments?
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Additional information
ALWAYS FOLLOW THE LABEL
What are sensitive teeth?
Lots of people have sensitive teeth. When enamel is worn away (through eating everyday acidic food or
drinks) or gums recede, the dentin underneath becomes exposed. This can lead to tooth sensitivity,
for example, with cold and hot food and drinks.
What does Sensodyne do?
Sensodyne provides daily care for sensitive teeth* plus all the benefits you would expect from a daily fluoride toothpaste - strong teeth and freshness.
*with twice daily brushing.
24/7 Sensitivity Protection*
+ Strong & Healthy Teeth
Use Sensodyne Advanced Whitening twice daily:
• Long lasting sensitivity protection* every day
• Contains fluoride to protect against cavities
Trademarks are owned by or licensed to the GSK group of companies.
©2020 GSK group of companies or its licensor.
Distributed by:
GSK Consumer Healthcare
Warren, NJ 07059
62000000057087
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SENSODYNE ADVANCED WHITENING
potassium nitrate pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0479 Route of Administration ORAL 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) SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) ALUMINUM OXIDE (UNII: LMI26O6933) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM HYDROXIDE (UNII: 55X04QC32I) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SUCRALOSE (UNII: 96K6UQ3ZD4) 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:0135-0479-01 1 in 1 CARTON 10/16/2020 1 184 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0135-0479-02 4 in 1 CARTON 07/03/2023 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 10/16/2020 Labeler - Haleon US Holdings LLC (079944263)
