Label: NATEAN CLEAN AND WHITEN- sodium fluoride paste
- NDC Code(s): 0135-1200-03
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 19, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
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adults and children 12 years of age and older:
- brush teeth thoroughly, preferably after each meal or at least twice a day, and not more than 3 times a day, or as recommended by a dentist or doctor. 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
- Questions or comments?
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Additional Information
ALWAYS FOLLOW THE LABEL
*No animal origin materials used in the processing of these products. Contains no animal ingredients or derivatives.
†Recycling facilities for this product may not exist in your area
Natean was created by a small passionate team of scientists and herbalists on a mission to give you the best of what nature and science can offer, while minimizing our impact to the planet. Our toothpastes expertly balance powerful, scientifically studied ingredients with botanicals for a clean you can feel, and a clean you can feel good about.
NATEAN-INSPIRED BY NATURE AND DESIGNED TO BE CLEAN
WHITENS TEETH AND LEAVES YOUR MOUTH FEELING CLEAN AND FRESH
- Our blend with pineapple and papaya extracts, and silica removes stains and whitens teeth
- Contains Fluoride to fight cavities
- Helps control tartar build-up with twice daily brushing
BPA-FREE TUBE
Tube contains post consumer recycled plastic
Recycleable carton, tube & cap
Distributed by: Alacer Corp.Carlisle, PA 17013
Made in Taiwan © 2021 Alacer Corp.
www.nateantoothpaste.com
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INGREDIENTS AND APPEARANCE
NATEAN CLEAN AND WHITEN
sodium fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-1200 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) SORBITOL (UNII: 506T60A25R) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG) XANTHAN GUM (UNII: TTV12P4NEE) REBAUDIOSIDE A (UNII: B3FUD0528F) MALTODEXTRIN (UNII: 7CVR7L4A2D) BROMELAINS (UNII: U182GP2CF3) PAPAIN (UNII: A236A06Y32) 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:0135-1200-03 1 in 1 CARTON 01/03/2022 1 133 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 01/03/2022 Labeler - Haleon US Holdings LLC (079944263)
