Label: NATURE MINT ANTICAVITY- sodium monofluorophosphate paste, dentifrice
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NDC Code(s):
53247-123-01,
53247-123-02,
53247-123-03,
53247-123-04, view more53247-123-05, 53247-123-06, 53247-123-07
- Packager: Bob Barker Company Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 31, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Use
- Warnings
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Directions
Adults & Children 6 years of age & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children 2 to 6 years: Use only a pea sized amount and supervise child's brushing and rinsing (to minimize swallowing). Children under 2 years: Ask a dentist or physician. - Inactive Ingredients
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 24 GRAM Tube Label
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INGREDIENTS AND APPEARANCE
NATURE MINT ANTICAVITY
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:53247-123 Route of Administration DENTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Sodium Monofluorophosphate (UNII: C810JCZ56Q) (Fluoride Ion - UNII:Q80VPU408O) Fluoride Ion 7.6 mg in 1 g Inactive Ingredients Ingredient Name Strength Calcium Carbonate (UNII: H0G9379FGK) WATER (UNII: 059QF0KO0R) Sorbitol (UNII: 506T60A25R) Glycerin (UNII: PDC6A3C0OX) Sodium Lauryl Sulfate (UNII: 368GB5141J) Hydrated Silica (UNII: Y6O7T4G8P9) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SODIUM PYROPHOSPHATE (UNII: O352864B8Z) Sodium Benzoate (UNII: OJ245FE5EU) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:53247-123-01 7.94 g in 1 PACKET; Type 0: Not a Combination Product 01/01/2008 2 NDC:53247-123-02 17 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2008 3 NDC:53247-123-03 24 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2008 4 NDC:53247-123-04 43 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2008 5 NDC:53247-123-05 78 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2008 6 NDC:53247-123-06 1 in 1 CARTON 01/01/2008 6 130 g in 1 TUBE; Type 0: Not a Combination Product 7 NDC:53247-123-07 1 in 1 CARTON 01/01/2008 7 181 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 01/01/2008 Labeler - Bob Barker Company Inc. (058525536)