Label: COLGATE TOTAL SF ADVANCED WHITENING- stannous fluoride paste, dentifrice
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NDC Code(s):
35000-178-14,
35000-178-18,
35000-178-25,
35000-178-47, view more35000-178-64, 35000-178-65, 35000-178-93
- Packager: Colgate-Palmolive Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 18, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purposes
- Uses
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Warnings
When using this product for sensitivity, do not use longer than 4 weeks unless recommended by a dentist.
Stop use and ask a dentist if the sensitivity problem persist or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist.
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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 bristled toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist.
Make sure to brush all sensitive areas of the teeth. - do not swallow.
- children under 12 years of age: consult a dentist.
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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 bristled toothbrush. Brush teeth thoroughly for at least 1 minute twice a day (morning and evening) or as recommended by a dentist.
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- Principal Display Panel - 181 g Tube Carton
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INGREDIENTS AND APPEARANCE
COLGATE TOTAL SF ADVANCED WHITENING
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:35000-178 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.1 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) HYDRATED SILICA (UNII: Y6O7T4G8P9) GLYCERIN (UNII: PDC6A3C0OX) POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9) SODIUM PYROPHOSPHATE (UNII: O352864B8Z) SODIUM LAURYL SULFATE (UNII: 368GB5141J) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) ZINC PHOSPHATE (UNII: 1E2MCT2M62) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SACCHARIN SODIUM (UNII: SB8ZUX40TY) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) XANTHAN GUM (UNII: TTV12P4NEE) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SUCRALOSE (UNII: 96K6UQ3ZD4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 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:35000-178-25 1 in 1 CARTON 05/14/2019 12/31/2022 1 24.9 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:35000-178-93 1 in 1 CARTON 05/14/2019 12/31/2022 2 96 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:35000-178-47 1 in 1 CARTON 05/14/2019 12/31/2022 3 144 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:35000-178-65 2 in 1 CARTON 05/14/2019 01/31/2023 4 144 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:35000-178-64 1 in 1 CARTON 05/14/2019 5 181 g in 1 TUBE; Type 0: Not a Combination Product 6 NDC:35000-178-14 1 in 1 CARTON 05/14/2019 03/31/2023 6 39.6 g in 1 TUBE; Type 0: Not a Combination Product 7 NDC:35000-178-18 5 in 1 CELLO PACK 03/20/2023 7 1 in 1 CARTON 7 181 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 M021 05/14/2019 Labeler - Colgate-Palmolive Company (001344381)