Label: FOAMING HAND- benzalkonium chloride soap

  • NDC Code(s): 83986-224-08, 83986-224-45, 83986-224-86
  • Packager: UpLift Brands, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 15, 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 thoroughly 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

    DISTRIBUTED BY:

    UPLIFT BRANDS, LLC

    ST. LOUIS, MO 63114

    1-866 MY GERMX

  • Principal display panel

    germ-X ®

    PRO

    ANTIBACTERIAL

    FOAMING

    HAND SOAP

    1000 ML (1.05 QT) 33.8 FL OZ

    image description

  • INGREDIENTS AND APPEARANCE
    FOAMING HAND 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-224
    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:83986-224-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/11/2024
    2NDC:83986-224-451150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/11/2024
    3NDC:83986-224-861000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product04/11/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/11/2024
    Labeler - UpLift Brands, LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-224)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-224)
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