Label: FOAMING ANTIBACTERIAL- benzalkonium chloride solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated July 25, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient

    Benzalkonium Chloride 0.13%

  • PURPOSE

    Purpose

    Antiseptic Handwash

  • INDICATIONS & USAGE

    Use

    • For handwashing to decrease bacteria on the skin
  • WARNINGS

    Warnings

    For external use only

  • DO NOT USE

    Do not use

    • In eyes
  • WHEN USING

    When using this product

    • If in eyes, rinse promptly and thoroughly with water
    • Discontinue use if irritation and redness develop
  • STOP USE

    Stop use and ask a doctor if

    • Skin irritation or redness occurs for more than 72 hours
  • 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

    • Wet hands and apply foam
    • Scrub hands and forearms
    • Rinse thoroughly and dry
  • OTHER SAFETY INFORMATION

    Other information

    • For additional information, see Safety Data Sheet (SDS)
    • For emergency medical information, call 1-866-767-5045
  • INACTIVE INGREDIENT

    Inactive ingredients Water, Caprylyl/Capryl Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance, Blue 1.

  • PRINCIPAL DISPLAY PANEL

    Member's Mark

    2 REFILLS

    FOAMING ANTIBACTERIAL

    HAND SOAP

    COMMERCIAL GRADE

    KILLS 99.99% OF GERMS*

    FRESH CLEAN FRAGRANCE

    KEEP OUT OF REACH OF CHILDREN.

    WARNING: CAUSES SERIOUS EYE

    IRRITATION (SEE BACK PANEL FOR DETAILS).

    2 REFILLS 33.8 FL OZ (1000mL) EACH

    TOTAL NET 67.6 FL OZ (2000mL)

    Package Label

    Inner Package

  • INGREDIENTS AND APPEARANCE
    FOAMING ANTIBACTERIAL 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68196-667
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)  
    WATER (UNII: 059QF0KO0R)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68196-667-022 in 1 BOX09/16/2024
    11000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/16/2024
    Labeler - Sam's West, Inc. (051957769)
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