Label: SOURCE ANTIBACTERIAL FOAMING HAND ORIGINAL- 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 February 21, 2013

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  • ACTIVE INGREDIENT


    Active Ingredient Purpose

    Triciosan 0.46% ********** Antibecterial

  • PURPOSE



    Decreases bacteria on the skin

  • KEEP OUT OF REACH OF CHILDREN

    avoid eye contact, if contact occurs rinse thoroughly with water.

  • INDICATIONS & USAGE

    Pump foam into hands, lather vigorously and rinse

  • WARNINGS

    For external use only.
    avoid eye contact, if contact occurs rinse thoroughly with water. If irritation occurs discontinue use of product.

  • DOSAGE & ADMINISTRATION

    Pump foam into hands, lather vigorously and rinse.

  • INACTIVE INGREDIENT

    Water, Sodium Laureth Sulfate, Dipropylene Glycol, Glycerin, Sodium PCA, Ammonium Lauryl Sulfate, Cocamidopropyl Betaire, Polyquaterium 10, Fragrance, Disodium Phosphate, Citric Acid, FD&C Red No. 4, FD&C Yellow No. 5

  • PRINCIPAL DISPLAY PANEL

    image of bottle label
  • INGREDIENTS AND APPEARANCE
    SOURCE ANTIBACTERIAL FOAMING HAND ORIGINAL 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64024-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.46 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    glycerin (UNII: PDC6A3C0OX)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64024-100-01222 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/04/2013
    Labeler - Aldi Inc. (944259522)
    Registrant - Ningbo Pulisi Daily Chemical Products Co., (529047265)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Pulisi Daily Chemical Products Co.,529047265manufacture(64024-100)
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