Label: NATURE MINT ANTICAVITY- sodium monofluorophosphate paste, dentifrice

  • NDC Code(s): 53247-131-01, 53247-131-02, 53247-131-03, 53247-131-04, view more
    53247-131-05, 53247-131-06, 53247-131-07
  • Packager: Bob Barker Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 18, 2024

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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, Glycerin, Silica, Sodium Lauryl Sulfate, Xanthan Gum, Flavor, Sodium Saccharin, Titanium Dioxide, Sodium Methylparaben, Sodium Propylparaben

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 43 Gram Tube Label

    Nature Mint®

    ANTICAVITY FLUORIDE TOOTHPASTE

    SODIUM MONOFLUOROPHOSPHATE - 0.76%

    FRESH MINT FLAVOR

    NET WT 1.5 OZ (43 GRAMS)

    PRINCIPAL DISPLAY PANEL - 43 Gram Tube Label
  • INGREDIENTS AND APPEARANCE
    NATURE MINT ANTICAVITY 
    sodium monofluorophosphate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-131
    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)  
    Glycerin (UNII: PDC6A3C0OX)  
    Silicon Dioxide (UNII: ETJ7Z6XBU4)  
    Sodium Lauryl Sulfate (UNII: 368GB5141J)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Saccharin Sodium (UNII: SB8ZUX40TY)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Methylparaben Sodium (UNII: CR6K9C2NHK)  
    Propylparaben Sodium (UNII: 625NNB0G9N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53247-131-017.94 g in 1 PACKET; Type 0: Not a Combination Product01/01/2023
    2NDC:53247-131-0217 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
    3NDC:53247-131-0324 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
    4NDC:53247-131-0443 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
    5NDC:53247-131-0578 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
    6NDC:53247-131-061 in 1 CARTON01/01/2023
    6130 g in 1 TUBE; Type 0: Not a Combination Product
    7NDC:53247-131-071 in 1 CARTON01/01/2023
    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 drugM02101/01/2023
    Labeler - Bob Barker Company Inc. (058525536)
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