Label: KIDS CREST CAVITY PROTECTION SPARKLE FUN- sodium fluoride paste, dentifrice
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NDC Code(s):
37000-049-01,
37000-049-02,
37000-049-03,
37000-049-04, view more37000-049-05, 37000-049-06, 37000-049-22, 37000-049-30, 37000-049-40, 37000-049-42, 37000-049-92
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 18, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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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
- adults and children 2 yrs. & older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist
- Inactive ingredients
- Questions?
- PRINCIPAL DISPLAY PANEL - 62 g carton
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INGREDIENTS AND APPEARANCE
KIDS CREST CAVITY PROTECTION SPARKLE FUN
sodium fluoride paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-049 Route of Administration DENTAL 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 SORBITOL (UNII: 506T60A25R) SACCHARIN SODIUM (UNII: SB8ZUX40TY) WATER (UNII: 059QF0KO0R) HYDRATED SILICA (UNII: Y6O7T4G8P9) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM PHOSPHATE (UNII: SE337SVY37) MICA (UNII: V8A1AW0880) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) Product Characteristics Color blue Score Shape Size Flavor BUBBLE GUM Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-049-03 2.5 g in 1 POUCH; Type 0: Not a Combination Product 09/05/2002 2 NDC:37000-049-01 1 in 1 CARTON 09/05/2002 2 24 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:37000-049-04 1 in 1 CARTON 09/05/2002 12/19/2016 3 77 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:37000-049-02 1 in 1 CARTON 09/05/2002 4 130 g in 1 TUBE; Type 0: Not a Combination Product 5 NDC:37000-049-06 170 g in 1 BOTTLE; Type 0: Not a Combination Product 09/05/2002 12/01/2018 6 NDC:37000-049-05 1 in 1 CARTON 09/05/2002 06/14/2019 6 76 g in 1 TUBE; Type 0: Not a Combination Product 7 NDC:37000-049-42 119 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 08/01/2017 8 NDC:37000-049-92 2 in 1 CELLO PACK 09/05/2002 8 1 in 1 CARTON 8 130 g in 1 TUBE; Type 0: Not a Combination Product 9 NDC:37000-049-22 1 in 1 CARTON 01/07/2019 9 62 g in 1 TUBE; Type 0: Not a Combination Product 10 NDC:37000-049-30 3 in 1 CELLO PACK 01/01/2021 10 1 in 1 CARTON 10 130 g in 1 TUBE; Type 0: Not a Combination Product 11 NDC:37000-049-40 1 in 1 CARTON 03/01/2022 11 119 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 09/05/2002 Labeler - The Procter & Gamble Manufacturing Company (004238200)