Label: POLIDENT PROPARTIAL- stannous fluoride paste
- NDC Code(s): 0135-0710-01, 0135-0710-02, 0135-0710-03
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 7, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purposes
- Uses
- Warnings
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Directions
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adults and children 2 years of age and older:
- apply toothpaste onto a toothbrush.
- brush teeth thoroughly, preferably after each meal at least twice a day, and not more than 3 times a day, or as directed by a dentist or doctor. Minimize swallowing. Spit out after brushing.
- to minimize swallowing for children under 6 years of age, use a pea-sized amount and supervise brushing and rinsing until good habits are established.
- children under 2 years of age:Consult a dentist or doctor.
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adults and children 2 years of age and older:
- Other information
- Inactive ingredients
- Questions or comments?
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Additional Information
ALWAYS FOLLOW THE LABEL
Your partial can act as a bacteria magnet, attracting more odor-causing bacteria, plaque and debris that if not cleaned can damage your natural teeth.
NEW POLIDENT ProPartialis a simple 3-step range specially developed to cleanse partial dentures, help strengthen teeth, and help protect against odor-causing bacteria.
STEP 1PURIFYYour Partial with Foam Cleanser
STEP 2 STRENGHTENYour Teeth + Gums with Toothpaste
STEP 3 PROTECTYour Teeth with Mouthwash
Strengthens by remineralizing teeth, including vulnerable teeth next to the partial and helps fight plaque bacteria*.
*associated with gingivitis, an early form of gum disease
1-866-844-2796
Distributed by:
GSK Consumer Healthcare,Warren, NJ 07059
Trademarks are owned by or licensed to the GSK group of companies.
©2020 GSK group of companies or its licensor.
Made in Germany.
Best used before the end of: see end of carton.
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INGREDIENTS AND APPEARANCE
POLIDENT PROPARTIAL
stannous fluoride pasteProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0710 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM TRIPOLYPHOSPHATE ANHYDROUS (UNII: 9SW4PFD2FZ) SODIUM LAURYL SULFATE (UNII: 368GB5141J) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-0710-01 1 in 1 CARTON 01/04/2021 1 96.4 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0135-0710-02 1 in 1 CARTON 01/04/2021 2 65.2 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:0135-0710-03 1 in 1 CARTON 01/04/2021 3 22.7 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 01/04/2021 Labeler - Haleon US Holdings LLC (079944263)