Label: TARGET UP AND UP ANTICAVITY- sodium fluoride 0.05% mouthwash

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • Drug Facts

  • Active ingredient

    Sodium Fluoride....... 0.05%

  • Purpose

    Anticavity

  • Uses

    Aids in the prevention of dental cavities

  • Warnings

    Keep out of reach of children.

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

  • Directions

    • Adults and Children 6 years of age and older:Use once a day after brushing your teeth with a toothpaste.
    • Vigorously swish 10 milliliters of rinse between your teeth for 1 minute and then spit out.
    • Do not swallow the rinse.
    • Do not eat or drink for 30 minutes after rinsing.
    • Instruct children under 12 years of age in good rinsing habits (to minimize swallowing).
    • Supervise children as necessary until capable of using without supervision.
    • Children under 6 years of age: consult a dentist or doctor.
  • Other information

    Do not use if the printed safety seal on the bottle's neck is broken or missing.

  • Inactive ingredients

    Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Sodium Benzoate, Sodium Bicarbonate, Disodium Phosphate, Sodium Chlorite, Menthol, Stevia Rebaudiana Extract, Flavor, Disodium EDTA, Xylitol, Citric Acid

  • PRINCIPAL DISPLAY PANEL

    Principal display panel

  • INGREDIENTS AND APPEARANCE
    TARGET UP AND UP ANTICAVITY 
    sodium fluoride 0.05% mouthwash
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-106
    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
    CALCIUM DISODIUM EDTA (UNII: 8U5D034955)  
    XYLITOL (UNII: VCQ006KQ1E)  
    PEG-40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SODIUM CHLORITE (UNII: G538EBV4VF)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DISODIUM PHOSPHATE (UNII: 22ADO53M6F)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-106-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product12/18/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02112/18/2024
    Labeler - TARGET CORPORATION (006961700)
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