Label: BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY- sodium fluoride liquid

  • NDC Code(s): 73928-021-01
  • Packager: Kingkey MBC Life Technology Group co., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 22, 2024

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

View All Sections
  • Active ingredient

    SODIUM FLUORIDE 0.03%

  • Purpose

    Anticavity

  • Uses

    helps protect teeth against cavities

  • Warnings

    Keep out of reach of children under 6 years of age. lf you accidentally swallow more than used for rinsing, seek professional help or contact a Poison Control Center immediately.

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    Adults and children 6 years and older:

    • Use daily after you brush your teeth with toothpaste
    • Rinse toothpaste from mouth prior to use.
    • Shake well before each use.Twist and remove cap.
    • Rinse or gargle for 30 seconds with 15 ml and spit out.
    • Do Notswallow the rinse.
    • Do Noteat or drink for 30 minutes after rinsing
    • Supervise children as necessary.
    • Children under 6 years of age, consult with a dentist or doctor.
  • Inactive ingredients

    Water, SORBITOL, GLYCERIN, XYLITOL, POTASSIUM SORBATE, SODIUM BENZOATE, PEG-40 HYDROGENATED CASTOR OIL, FLAVOR
    SODIUM FLUORIDE, SODIUM SACCHARIN, CETYLPYRIDINIUM CHLORIDE, SUCRALOSE, CITRIC ACID, METHYL DIISOPROPYL PROPIONAMIDE
    D&C Red No.33（CI 17200, FD&C RED NO. 40

  • Questions or comments?

    Call toll free 1-877-274-8358

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    BRUSH BUDDIES HOTWHEEL ANTICAVITY FLUORIDE STRAWBERRY 
    sodium fluoride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73928-021
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.03 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SORBITOL (UNII: 506T60A25R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    XYLITOL (UNII: VCQ006KQ1E)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73928-021-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product05/10/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02105/10/2024
    Labeler - Kingkey MBC Life Technology Group co., LTD. (545349263)
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!