Label: DT ANTIBACTERIAL FOAMING HAND WASH- triclosan 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 December 22, 2010

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  • ACTIVE INGREDIENT

    Active Ingredient

    Triclosan 0.15%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses:

    for hand washing to decrease bacteria on the skin.

  • WARNINGS

    Warnings for external use only.

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor if 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 hands

    lather vigorously for at least 15 seconds

    rinse and dry thoroughly.

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water (aqua), sodium laureth sulfate, cocamide DEA, cocamidopropyl betaine, glycerin, citric acid, kathom CG, Fragrance, FD and C yellow No.5, FDandC Red No 40.

  • PRINCIPAL DISPLAY PANEL

    DT for your Daily Touch
    Antibacterial
    foaming Hand Wash

    Distributed by DT Products
    Vernon, CA 90058
    MADE IN CHINA
  • PRINCIPAL DISPLAY PANEL

    DT Antibacterial Hand Soap

  • INGREDIENTS AND APPEARANCE
    DT ANTIBACTERIAL FOAMING HAND WASH 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50523-632
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.15 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50523-632-08221 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/22/2010
    Labeler - Volume Distributors, Inc. (002029544)
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