Label: FOAMING HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 83986-118-44, 83986-118-45, 83986-118-86, 83986-118-96
  • Packager: UpLift Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 29, 2024

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  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antiseptic

  • Use

    to decrease bacteria on the skin

  • Warnings

    For external use only: hands only

  • When using this product

    • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
  • Stop use and ask a doctor if

    • if irritation and 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 thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants
  • Inactive ingredients

    cetrimonium chloride, diglycerin, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, sodium benzoate, tetrasodium EDTA, water

  • Claims

    *Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

    Made in USA with US and foreign parts

  • Adverse reactions

    Distributed By: Vi-Jon, Inc.

    8515 Page Ave, St. Louis, MO 63114

  • Principal display panel

    germ-X

    alcohol free

    foaming hand sanitizer

    Kills 99.99% of Germs*

    Fresh Scent

    7.5 FL OZ (221 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    FOAMING HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-118
    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
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    DIGLYCERIN (UNII: 3YC120743U)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE (UNII: 4M7P1JZ2V2)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-118-96221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
    2NDC:83986-118-44532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
    3NDC:83986-118-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
    4NDC:83986-118-451150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/29/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/29/2024
    Labeler - UpLift Brands LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-118)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-118)
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