Label: CREST PRO HEALTH CLEAN MINT- stannous fluoride paste, dentifrice
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NDC Code(s):
69423-781-03,
69423-781-33,
69423-781-43,
69423-781-44, view more69423-781-45, 69423-781-46, 69423-781-59, 69423-781-63, 69423-781-73, 69423-781-85
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 6, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Purposes
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Uses
- aids in the prevention of cavities
- helps prevent gingivitis
- helps interfere with the harmful effects of plaque associated with gingivitis
- helps control plaque bacteria that contribute to the development of gingivitis
- builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets, or contact
- WARNINGS
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Directions
- adults and children 12 yrs. & 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) or as recommended by a dentist. Make sure to brush all sensitive areas of the teeth.
- do not swallow
- children under 12 yrs. of age: ask a dentist
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- Principal Display Panel - 144 g tube in carton
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INGREDIENTS AND APPEARANCE
CREST PRO HEALTH CLEAN MINT
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-781 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 SODIUM GLUCONATE (UNII: R6Q3791S76) STANNOUS CHLORIDE (UNII: 1BQV3749L5) SUCRALOSE (UNII: 96K6UQ3ZD4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SORBITOL (UNII: 506T60A25R) GLYCINE (UNII: TE7660XO1C) SODIUM CITRATE (UNII: 1Q73Q2JULR) CARRAGEENAN (UNII: 5C69YCD2YJ) ZINC CITRATE (UNII: K72I3DEX9B) SODIUM HYDROXIDE (UNII: 55X04QC32I) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color blue Score Shape Size Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-781-59 1 in 1 CARTON 10/03/2022 1 167 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69423-781-85 1 in 1 CARTON 10/03/2022 2 24 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:69423-781-43 1 in 1 CARTON 10/03/2022 3 121 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:69423-781-44 3 in 1 CARTON 10/03/2022 4 121 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:69423-781-45 2 in 1 CARTON 10/03/2022 5 121 g in 1 TUBE; Type 0: Not a Combination Product 6 NDC:69423-781-73 1 in 1 CARTON 10/03/2022 6 73 g in 1 TUBE; Type 0: Not a Combination Product 7 NDC:69423-781-03 1 in 1 CARTON 10/03/2022 7 85 g in 1 TUBE; Type 0: Not a Combination Product 8 NDC:69423-781-46 1 in 1 CARTON 10/03/2022 8 130 g in 1 TUBE; Type 0: Not a Combination Product 9 NDC:69423-781-63 1 in 1 CARTON 10/03/2022 9 178 g in 1 TUBE; Type 0: Not a Combination Product 10 NDC:69423-781-33 1 in 1 CARTON 10/03/2022 10 94 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 10/03/2022 Labeler - The Procter & Gamble Manufacturing Company (004238200)