Label: KINDFILL- mint toothpaste tablets tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated August 10, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Active Ingredient(s)

    Sodium Fluoride .62mg (28 mg flouride ion)

  • Purpose

    Anti-cavity

  • Use

    aids in the prevention of dental cavities

  • Warnings

    • When using this product, if irritation or sensitivity occurs discontinue use.
    • Keep out of the reach of children. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.
  • WHEN USING

    When using this product, if irritation or sensitivity occurs discontinue use.

  • KEEP OUT OF REACH OF CHILDREN

    If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • Adults and children 6 years of age and older; chew one tablet until crushed, wet toothbrush, brush for 2 minutes. Spit out.
    • Do not swallow the tablet.
    • Children under 6 years of age should be supervised when using this product.
  • Other information

    Store at 25-30°C (68-77°F). Protect from excessive moisture.

  • Inactive ingredients

    Microcrystalline Cellulose, Sodium bicarbonate (Baking Soda), Silica, Sodium Lauryl Glutamate, Magnesium Stearate, Natural Mint Flavor, Menthol, Xanthan Gum, Stevia (Stevioside), Citric Acid

  • Package Label - Principal Display Panel

    60 in Each Box NDC: 80486-111-11

    60 in Each Box NDC: 80487-321-11

  • INGREDIENTS AND APPEARANCE
    KINDFILL 
    mint toothpaste tablets tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80487-321(NDC:68984-122)
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.62 mg
    Inactive Ingredients
    Ingredient NameStrength
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    STEVIA LEAF (UNII: 6TC6NN0876)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MINT (UNII: FV98Z8GITP)  
    MENTHOL, (+)- (UNII: C6B1OE8P3W)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize10mm
    FlavorPEPPERMINTImprint Code NONE
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80487-321-1160 in 1 BOX; Type 0: Not a Combination Product01/05/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35501/05/2023
    Labeler - By Humankind Inc (117642980)
    Establishment
    NameAddressID/FEIBusiness Operations
    Identipak, Inc942862350repack(80487-321)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!