Label: FRESHMINT ANTICAVITY FLUORIDE- sodium monofluorophosphate paste, dentifrice
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NDC Code(s):
51824-067-01,
51824-067-02,
51824-067-03,
51824-067-04, view more51824-067-05, 51824-067-06, 51824-067-07, 51824-067-08, 51824-067-09
- Packager: New World Imports, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 29, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Adults and Children 6 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or physician.
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 of physician.
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FRESHMINT ANTICAVITY FLUORIDE
sodium monofluorophosphate paste, dentifriceProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51824-067 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) Silicon Dioxide (UNII: ETJ7Z6XBU4) Sodium Lauryl Sulfate (UNII: 368GB5141J) Carboxymethylcellulose Sodium (UNII: K679OBS311) Sodium Silicate (UNII: IJF18F77L3) Sodium phosphate, tribasic, dodecahydrate (UNII: B70850QPHR) Saccharin Sodium (UNII: SB8ZUX40TY) Methylparaben (UNII: A2I8C7HI9T) Titanium Dioxide (UNII: 15FIX9V2JP) Polyethylene Glycol 400 (UNII: B697894SGQ) Propylparaben (UNII: Z8IX2SC1OH) Product Characteristics Color white (White) Score Shape Size Flavor MINT (Mint) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51824-067-01 17 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 2 NDC:51824-067-02 17 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 3 NDC:51824-067-03 24 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 4 NDC:51824-067-04 43 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 5 NDC:51824-067-05 43 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 6 NDC:51824-067-06 78 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 7 NDC:51824-067-07 78 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 8 NDC:51824-067-08 130 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 9 NDC:51824-067-09 181 g in 1 TUBE; Type 0: Not a Combination Product 09/16/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M021 09/16/2010 Labeler - New World Imports, Inc (075372276)