Label: THE HUMBLE CO. ANTICAVITY FRESH MINT- sodium fluoride paste, dentifrice

  • NDC Code(s): 72299-019-01
  • Packager: The Humble Company North America, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Drug Facts

  • Active ingredient

    Sodium fluoride 0.243% (0.15% w/v fluoride ion)

    Purpose

    Anticavity Toothpaste

  • Use

    aids in the prevention of dental cavities

  • Warning

    Keep out of 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 right away.

  • Directions

     Adults and children 2 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 doctor.
     Children under 6 years of age Instruct in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.
     Children under 2 years of age Consult a dentist or doctor.

  • Other information

    store below 25°C (77°F)

  • Inactive ingredients

    sorbitol, water, hydrated silica, xylitol, lauryl glucoside, xanthan gum, peppermint (mentha x piperita l.) oil, titanium dioxide, cocamidopropyl betaine, flavor, rebaudioside A, aloe vera (aloe barbadensis) leaf juice, charcoal powder, sodium benzoate, potassium sorbate, limonene, citric acid.

  • Questions?

    Call (619) 940-6502

  • Package Labeling:

    Box Label2Label2

  • INGREDIENTS AND APPEARANCE
    THE HUMBLE CO. ANTICAVITY FRESH MINT 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72299-019
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    XYLITOL (UNII: VCQ006KQ1E)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    REBAUDIOSIDE A (UNII: B3FUD0528F)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72299-019-011 in 1 CARTON09/01/202108/31/2023
    1175 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02109/01/202108/31/2023
    Labeler - The Humble Company North America, Inc (010966342)
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