Label: FOAMING HAND WASH- triclosan 0.46% liquid

  • 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 May 3, 2013

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  • Active ingredient

    Triclosan 0.46%

  • Purpose

    Antibacterial

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only - hands only

  • When using this product

    avoid contact with the eyes. If contact occurs, rinse eyes with water

  • Stop use and ask a doctor if

    irritation or redness develops

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control center right away.

  • Directions

    • wet hands
    • apply palmful to hands
    • scrub thoroughly
    • rinse thoroughly
  • Inactive ingredients

    water, sodium laureth sulfate, glcerin, cocamidopropyl betaine, ammonium xylenesulfonate, fragrance, disodium phosphate, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisothiazolinone, red 4, yellow 5

  • adverse reactions

    Distributed  by Target Corp., Mpls., MN 55403

    Made in the U.S.A. with U.S. and foreign components

    Shop Target.com

    Guest Services 1-800-910-6874

  • Principal Display Panel

    foaming

    hand wash

    antibacterial

    helps fight germs

    Loaded lather

    up+up

    7.5 FL OZ (221.8 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    FOAMING HAND WASH 
    triclosan 0.46% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-962
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN.46 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-962-96221.8 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/10/2012
    Labeler - Target Corp (006961700)
    Registrant - Vi-Jon (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon088520668manufacture(11673-962)
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