Label: BARRICADE- benzalkonium chloride soap

  • 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 September 11, 2020

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  • ACTIVE INGREDIENT

    Benzalkonium Chloride 0.2%

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • INACTIVE INGREDIENT

    water, lauramine oxide, coco-betaine, cocamide diisopropylamine, glycerin, methylchloroisothiazolinone, methylisothi- azolinone, citric acid, lemon oil, ethyl hydroxyethyl cellulose

  • DOSAGE & ADMINISTRATION

    For maximum efficiency, pump the product into wet hands, lather vigorously, sinse and dry.

  • INDICATIONS & USAGE

    For hand washing to decrease bacteria that can potentially cause disease.

  • WARNINGS

    For external use only.
    Do Not Use in children less than 2 months of age or on open skin wounds

  • OTHER SAFETY INFORMATION

    . Store between 15°C – 30° C (59°F - 86°F)

    . Avoid from freezing and excessive heat above 40°C (104°F)

  • PURPOSE

    Antiseptic

  • PRINCIPAL DISPLAY PANEL

    BARRICADE BOX LABELBARRICADE GALLON LABEL

  • INGREDIENTS AND APPEARANCE
    BARRICADE 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77075-079
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%) (UNII: X70SE62ZAR)  
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)  
    WATER (UNII: 059QF0KO0R)  
    LEMON OIL (UNII: I9GRO824LL)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77075-079-044 in 1 BOX09/11/2020
    1NDC:77075-079-013784 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/11/2020
    Labeler - Eaton Chemical, Inc. (056388804)
    Establishment
    NameAddressID/FEIBusiness Operations
    R. N. Eaton & Company, Inc.056388804manufacture(77075-079)
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