Label: WALGREENS ANTICAVITY AND ANTIGINGIVITS WHITENING FLUORIDE TOOTHPASTE- anticavity and antigingivitis whitening fluoride paste, dentifrice

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated November 5, 2009

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  • ACTIVE INGREDIENTS

    Sodium Fluoride 0.234% (0.15% w/v fluoride ion..........................Anticavity toothpaste

  • Use:

    Helps protect against cavities.

  • WARNINGS

    As with all fluoride toothpastes, keep out of reach of children under 6 years of age.  If you accidentally swallow more than used for brushing, seek professional help or contact the Poison Control Center immediately.


  • DOSAGE & ADMINISTRATION

    Adults and children 6 years or older
    		Brush Teeth throughly, preferably after each meal, or at least twice a day, or as directed by your dentist.  Do not swallow

    Children between 6 and 12 yearsTo minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.
    Children under 6 years Ask a dentist or physician.

  • Inactive Ingredients

    Sorbitol, Silica, Water, Glycerin, Sodium Laurel Sulphate, Zinc Citrate, Titanium Dioxide, Cellulose Gum, Flavor, PVP, Sodium Benzoate, Tetrasodium Pyrophosphate, Sodium Saccharine, Sodium Hydroxide, Carrageenan, Mica, FDC Blue No. 1.

  • Principal Display Panel

    Anticavity and Antigingivitis                                                         Compare to Colgate

    WHITENING                        

    Fluoride Toothpaste                                                                     Fights Tartar  

                                                             Build-up
    NET WT 6.4 oz (181.4 g)                                                              Whitens Teeth

    image of container


  • INGREDIENTS AND APPEARANCE
    WALGREENS ANTICAVITY AND ANTIGINGIVITS WHITENING FLUORIDE TOOTHPASTE 
    anticavity and antigingivitis whitening fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67659-062
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Sodium Fluoride (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) Sodium Fluoride2.43 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Sorbitol (UNII: 506T60A25R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    Zinc Citrate (UNII: K72I3DEX9B)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Carrageenan (UNII: 5C69YCD2YJ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67659-062-66181.4 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved other11/24/2008
    Labeler - Team Technologies, Inc (192339703)
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