Label: GOJO E2 FOAM SANITIZING S OAP CHLOROXYLENOL LIQUID- chloroxylenol liquid

  • NDC Code(s): 21749-565-20, 21749-565-89, 21749-565-90
  • Packager: GOJO Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated July 30, 2017

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  • PRINCIPAL DISPLAY PANEL

    Product LabelProduct LabelProduct Label

  • INGREDIENTS AND APPEARANCE
    GOJO E2 FOAM SANITIZING S OAP CHLOROXYLENOL LIQUID 
    chloroxylenol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21749-565
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.01 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALCOHOL (UNII: 3K9958V90M)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    AMMONIUM LAURETH-5 SULFATE (UNII: 43ZIH89I48)  
    Ammonium Xylenesulfonate (UNII: 4FZY6L6XCM)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    Glycerin (UNII: PDC6A3C0OX)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    AMMONIUM SULFATE (UNII: SU46BAM238)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21749-565-891200 mL in 1 PACKAGE; Type 0: Not a Combination Product06/15/2014
    2NDC:21749-565-901250 mL in 1 PACKAGE; Type 0: Not a Combination Product09/30/2005
    3NDC:21749-565-202000 mL in 1 PACKAGE; Type 0: Not a Combination Product09/30/2005
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    export only09/30/2005
    Labeler - GOJO Industries, Inc. (004162038)
    Establishment
    NameAddressID/FEIBusiness Operations
    GOJO Industries, Inc.036424534MANUFACTURE(21749-565)