Label: SENSODYNE NOURISH GENTLY SOOTHING- potassium nitrate and sodium fluoride paste
- NDC Code(s): 0135-5026-01, 0135-5026-02, 0135-5026-03
- 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:
- 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: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 FOLLOW THE LABEL
SENSODYNE nourish
WITH BIO-ACTIVE MINERALS
Brush twice daily for a healthier smile:
- Strengthens & nourishes teeth
- Helps prevent cavities
- Protects from sensitivity*
- Freshens breath
The Sensodyne Nourish rangewith bio-active minerals, strengthens and nourishes teeth while also protecting from sensitivity*. Our toothpaste is designed to provide the everyday nourishment your teeth to help protect the health of your mouth.
Gently Soothing:With trusted sensitivity protection*, our formulation, blended with aloe vera extract and natural mint, is designed for a clean sensation.
*with twice daily brush
Help us support the planet by recycling our packaging and being responsible with water usage.
CARTON
RECYCLE
TUBE
RECYCLE
LOT
See end of carton
Save Water
Turn off tap whilst 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 NOURISH GENTLY SOOTHING
potassium nitrate and sodium fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-5026 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 SACCHARIN SODIUM (UNII: SB8ZUX40TY) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) COCONUT OIL (UNII: Q9L0O73W7L) SODIUM LAURYL SULFATE (UNII: 368GB5141J) XANTHAN GUM (UNII: TTV12P4NEE) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) 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:0135-5026-01 1 in 1 CARTON 01/03/2022 1 113 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0135-5026-02 1 in 1 CARTON 03/25/2022 2 23 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:0135-5026-03 23 g in 1 TUBE; Type 0: Not a Combination Product 01/02/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 01/03/2022 Labeler - Haleon US Holdings LLC (079944263)