Label: FOAMING HAND- benzalkonium chloride lotion

  • NDC Code(s): 11344-224-04, 11344-224-08, 11344-224-20, 11344-224-44, view more
    11344-224-45, 11344-224-86, 11344-224-96
  • Packager: Consumer Product Partners, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 11, 2024

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  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antibacterial

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only: hands only

  • When using this product

    avoid contact with eyes. If contact occurs, rinse eyes with water.

  • Stop use and ask a doctor if

    • irritation or redness develop
    • condition persists for more than 72 hours
  • Keep out of reach of children.

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

  • Directions

    • wet hands 
    • apply palmful to hands 
    • scrub thoroughly 
    • rinse thoroughly
  • Inactive ingredients

    water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA, sodium benzoate

  • Adverse event

    Manufactured By: Vi-Jon, Inc.

    St. Louis, Mo 63114

  • Adverse event

    germ-X

    Professional

    ANTIBACTERIAL

    FOAMING

    HAND SOAP

    1000 ML (33.8 FL OZ)

    image description

  • INGREDIENTS AND APPEARANCE
    FOAMING HAND 
    benzalkonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-224
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11344-224-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2018
    2NDC:11344-224-96222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/08/201804/11/2024
    3NDC:11344-224-44532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/201802/24/2021
    4NDC:11344-224-04750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/201804/11/2024
    5NDC:11344-224-451150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2018
    6NDC:11344-224-2044 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/08/201804/11/2024
    7NDC:11344-224-861000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/08/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/08/2018
    Labeler - Consumer Product Partners, LLC (119091520)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(11344-224)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(11344-224)
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