Label: CREST PRO-HEALTH ADVANCED GUM RESTORE DEEP CLEAN- stannous fluoride paste, dentifrice
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NDC Code(s):
69423-925-27,
69423-925-37,
69423-925-52,
69423-925-63, view more69423-925-85
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 11, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Purposes
- Uses
- Warning
- Directions
- KEEP OUT OF REACH OF CHILDREN
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- Principal Display Panel - 104 g tube in carton
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INGREDIENTS AND APPEARANCE
CREST PRO-HEALTH ADVANCED GUM RESTORE DEEP CLEAN
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-925 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength STANNOUS FLUORIDE (UNII: 3FTR44B32Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.4 mg in 1 g Inactive Ingredients Ingredient Name Strength GLYCINE (UNII: TE7660XO1C) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SUCRALOSE (UNII: 96K6UQ3ZD4) STANNOUS CHLORIDE (UNII: 1BQV3749L5) WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) CARRAGEENAN (UNII: 5C69YCD2YJ) SODIUM GLUCONATE (UNII: R6Q3791S76) XANTHAN GUM (UNII: TTV12P4NEE) ZINC CITRATE (UNII: K72I3DEX9B) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SORBITOL (UNII: 506T60A25R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SACCHARIN SODIUM (UNII: SB8ZUX40TY) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) SODIUM CITRATE (UNII: 1Q73Q2JULR) Product Characteristics Color white Score Shape Size Flavor PEPPERMINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-925-37 1 in 1 CARTON 01/04/2021 1 104 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69423-925-85 1 in 1 CARTON 01/04/2021 07/17/2023 2 24 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:69423-925-52 1 in 1 CARTON 12/01/2021 07/17/2023 3 147 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:69423-925-27 1 in 1 CARTON 01/01/2022 4 76 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:69423-925-63 3 in 1 CELLO PACK 01/04/2021 5 1 in 1 CARTON 5 104 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 01/04/2021 Labeler - The Procter & Gamble Manufacturing Company (004238200)