Label: NATURE MINT ANTICAVITY- sodium monofluorophosphate paste, dentifrice

  • NDC Code(s): 53247-123-01, 53247-123-02, 53247-123-03, 53247-123-04, view more
    53247-123-05, 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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  • SPL UNCLASSIFIED SECTION

    Drug Facts:

  • Active ingredient

    Sodium Monofluorophosphate - 0.76% (0.1% w/v fluoride ion)

  • Purpose

    Anticavity toothpaste

  • Use

    Helps protect against cavities.

  • Warnings

    Keep out of the reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

  • 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

    Calcium Carbonate, Water, Sorbitol, Glycerin, Sodium Lauryl Sulfate, Hydrated Silica, Cellulose Gum, Flavor, Sodium Saccharin, Tetrasodium Pyrophosphate, Sodium Benzoate

  • SPL UNCLASSIFIED SECTION

    Dist. by Bob Barker Co. Inc. Fuquay-Varina, NC 27526

  • PRINCIPAL DISPLAY PANEL - 24 GRAM Tube Label

    Nature Mint®

    ANTICAVITY FLUORIDE TOOTHPASTE

    SODIUM MONOFLUOROPHOSPHATE - 0.76%

    FRESH MINT FLAVOR

    NET WT 0.85 OZ (24 GRAMS)

    PRINCIPAL DISPLAY PANEL - 24 GRAM Tube Label
  • INGREDIENTS AND APPEARANCE
    NATURE MINT ANTICAVITY 
    sodium monofluorophosphate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-123
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Sodium Monofluorophosphate (UNII: C810JCZ56Q) (Fluoride Ion - UNII:Q80VPU408O) Fluoride Ion7.6 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53247-123-017.94 g in 1 PACKET; Type 0: Not a Combination Product01/01/2008
    2NDC:53247-123-0217 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
    3NDC:53247-123-0324 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
    4NDC:53247-123-0443 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
    5NDC:53247-123-0578 g in 1 TUBE; Type 0: Not a Combination Product01/01/2008
    6NDC:53247-123-061 in 1 CARTON01/01/2008
    6130 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:53247-123-071 in 1 CARTON01/01/2008
    7181 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM02101/01/2008
    Labeler - Bob Barker Company Inc. (058525536)
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