Label: CREST GUM AND ENAMEL REPAIR ADVANCED WHITENING- stannous fluoride paste, dentifrice
-
NDC Code(s):
37000-506-03,
37000-506-26,
37000-506-28,
37000-506-37, view more37000-506-41
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 17, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 - 116 g tube in carton
-
INGREDIENTS AND APPEARANCE
CREST GUM AND ENAMEL REPAIR ADVANCED WHITENING
stannous fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-506 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 STANNOUS CHLORIDE (UNII: 1BQV3749L5) WATER (UNII: 059QF0KO0R) SUCRALOSE (UNII: 96K6UQ3ZD4) 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) 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:37000-506-41 1 in 1 CARTON 04/01/2018 1 116 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:37000-506-03 3 in 1 CELLO PACK 04/01/2018 2 1 in 1 CARTON 2 116 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:37000-506-28 1 in 1 CARTON 02/03/2020 3 79 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:37000-506-37 1 in 1 CARTON 04/01/2018 4 104 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:37000-506-26 1 in 1 CARTON 04/01/2018 5 73 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 04/01/2018 Labeler - The Procter & Gamble Manufacturing Company (004238200)