Label: MOISTURIZING HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 83986-849-08, 83986-849-16, 83986-849-34, 83986-849-45
  • Packager: UpLift Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 1, 2024

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  • Active ingredient

    Ethyl alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • Warnings

    For exterenal use only: hands

    Flammable, keep away from fire or flame.

  • When using this product

    • keep out of eyes. In case of contact with eyes, flush thoroghly with water.
    • avoid contact with broken skin
    • do not inhale or ingest
  • Stop use and ask a doctor 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
  • Other information

    • do not store above 105⁰F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

  • Claims

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

    FORMULA MADE IN USA

    EMPLOYEE OWNED

  • Adverse reaction

    Distributed By Vi-Jon, LLC

    St. Louis, MO 63114

    www.germx.com

  • Principal panel display

    NEW LOOK!

    SAME FORMULA

    germ-X

    SINCE 1997

    ORINGINAL

    MOISTURIZING HAND SANITIZER

    Kills 99.99% of Germs*

    with vitamin E

    8 FL OZ (236 ML)

    image description

  • INGREDIENTS AND APPEARANCE
    MOISTURIZING HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-849
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-849-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2024
    2NDC:83986-849-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2024
    3NDC:83986-849-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2024
    4NDC:83986-849-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/01/2024
    Labeler - UpLift Brands, LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-849)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-849)
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