Label: DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH HELLO KITTY- triclosan solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 January 18, 2013

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  • ACTIVE INGREDIENT

    Active Ingredient - TRICLOSAN 0.46%

  • PURPOSE

    Antibacterial

  • INDICATIONS & USAGE

    For hand washing to decrease bacteria on the skin


  • WARNINGS

    For external use only.

  • STOP USE

    Stop use and ask a doctor if irritation and redness develops.

  • WHEN USING

    When using this product avoid contact with eyes.  In case of eye contact, flush with water.
  • ASK DOCTOR

    Stop use and ask a doctor irritation and redness develops.


  • KEEP OUT OF REACH OF CHILDREN


    Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions: Pump into dry hands. Lather vigorously for 15 seconds. Rinse and dry thoroughly.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Sodium Xylenesulfonate, Dipropylene Glycol, Glycerin, Sodium PCA, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Polyquaternium-10, Fragrance, Disodium Phosphate, Cetyl Alcohol, Aloe Barbadensis Leaf juice, Citric Acid, Methylparaben, Propylparaben

  • QUESTIONS

    Questions? 1-800-258-DIAL

  • PRINCIPAL DISPLAY PANEL

    Label image

    label image

  • INGREDIENTS AND APPEARANCE
    DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH  HELLO KITTY
    triclosan solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54340-810
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.46 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54340-810-01221 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/15/2012
    Labeler - The Dial Corporation (070252531)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Dial Corporation, West Hazelton825091622manufacture(54340-810)
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