Label: ANTIBACTERIAL HAND- triclosan liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 June 1, 2012

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  • SPL UNCLASSIFIED SECTION

    LIQUID
    HAND SOAP
  • ACTIVE INGREDIENT

    Active Ingredient
    Triclosan 0.15%

    Purpose
    Antibacterial
  • INDICATIONS & USAGE

    Uses for handwashing to decrease bacteria on the skin
  • WARNINGS

    Warnings
    For external use only.

    When using this product •do not get into eyes.  If contact occurs rinse eyes thoroughly 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.
  • DOSAGE & ADMINISTRATION

    Directions • wet hands •apply palmful to hands •scrub thoroughly •rinse
  • INACTIVE INGREDIENT

    Inactive ingredients  water, sodium laureth sulfate, sodium, lauryl sulfate, cocamidopropyl betaine, sodium chloride, decyl glucoside, glycerin,
    PEG-18 glyceryl oleate/cocoate, fragrance, cocamide MEA, DMDM hydantoin, tetrasodium EDTA, citric acid, yellow 5, red 4
  • SPL UNCLASSIFIED SECTION

      This product is not manufactured or distributed by The Dial Corporation, distributor of Dial Gold Antibacterial Soap
  • ADVERSE REACTIONS

    SATISFACTION GUARANTEED OR YOUR MONEY BACK
    Manufactured For Your Military Exchanges
    By Vi-Jon
    8515 Page Ave
    St. Louis, Mo 63114
    image of principal display panel
  • PRINCIPAL DISPLAY PANEL

    Exchange
    Select
    LIQUID
    HAND SOAP
    ANTIBACTERIAL
    Compare to Dial Gold
    Antibacterial Soap
    Refill
    15 FL OZ (443 mL)
    image of principal display panel
  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55301-243
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.15 kg  in 100 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG-18 GLYCERYL OLEATE/COCOATE (UNII: VD2D270332)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55301-243-49.443 L in 1 BOTTLE, PLASTIC
    2NDC:55301-243-971.89 L in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333A01/06/2009
    Labeler - Your Military Exchange (001695568)
    Registrant - Vi-Jon (088520668)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon088520668manufacture
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