Label: ANTICAVITY FLUORIDE- sodium fluoride liquid

  • NDC Code(s): 73928-090-01
  • Packager: Kingkey MBC Life Technology Group co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 1, 2024

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  • Active ingredient

    SODIUM FLUORIDE 0.05%

  • Puropse

  • Uses

    helps protect teeth against cavities.

  • Warnings

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

  • WARNINGS

    Keep out of reac of children under 6 years of age. lf youaccidentally swallow more than used for rinsing, seek professionahelp or contact a Poison Control Center immediately.

  • 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 Not swallow the rinse.
    Do Not eat 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
    SODIUM BENZOATE
    PEG-40 HYDROGENATED CASTOR OIL
    POTASSIUM SORBATE
    FLAVOR
    SODIUM SACCHARIN
    CETYLPYRIDINIUM CHLORIDE
    METHYL DIISOPROPYL PROPIONAMIDE
    SUCRALOSE
    CITRIC ACID

    FD&C Yellow No.5（CI 19140）
    FD&C Blue No.1（CI 42090）

  • Questions or comments?

    Call toll free 0755-89203021

  • label

    label

  • INGREDIENTS AND APPEARANCE
    ANTICAVITY FLUORIDE 
    sodium fluoride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73928-090
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE0.05 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    XYLITOL (UNII: VCQ006KQ1E)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    WATER (UNII: 059QF0KO0R)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73928-090-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product12/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02112/01/2024
    Labeler - Kingkey MBC Life Technology Group co., LTD (545349263)
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