Label: CREST 3D WHITE STAIN ERASER POLISHING MINT- sodium fluoride paste, dentifrice
- NDC Code(s): 69423-958-32, 69423-958-33, 69423-958-36, 69423-958-63
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 18, 2023
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- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Use
- WARNINGS
- Warning
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Directions
- adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
- do not swallow
- to minimize swallowing use a pea-sized amount in children under 6
- supervise children's brushing until good habits are established
- children under 2 yrs.: ask a dentist
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- Crest 3D White Stain Eraser Polishing Mint
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INGREDIENTS AND APPEARANCE
CREST 3D WHITE STAIN ERASER POLISHING MINT
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-958 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 1.5 mg in 1 g Inactive Ingredients Ingredient Name Strength POLYSORBATE 80 (UNII: 6OZP39ZG8H) HYDRATED SILICA (UNII: Y6O7T4G8P9) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) SORBITOL (UNII: 506T60A25R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM HYDROXIDE (UNII: 55X04QC32I) CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC) SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD) WATER (UNII: 059QF0KO0R) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) MICA (UNII: V8A1AW0880) 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:69423-958-32 1 in 1 CARTON 07/09/2021 1 87 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69423-958-36 1 in 1 CARTON 07/09/2019 07/13/2023 2 99 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:69423-958-63 2 in 1 CELLO PACK 07/09/2021 3 1 in 1 CARTON 3 87 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:69423-958-33 3 in 1 CELLO PACK 01/01/2023 4 1 in 1 CARTON 4 87 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 07/09/2019 Labeler - The Procter & Gamble Manufacturing Company (004238200)