Label: HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 83986-815-16, 83986-815-34
  • Packager: UpLift Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 29, 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 external 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 thoroughly 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 105⁰ F
    • may discolor some fabrics 
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, PEG-6, glycerin, Glycine soja (soybean) oil, butylene glycol, Butyrospermum parkii (shea) butter, dimethicone, Aloe barbadensis leaf juice, acrylates/vinyl isodecanoate crosspolymer, fragrance, aminomethyl propanol, styrene/acrylates copolymer, xanthan gum, tocopheryl acetate

  • Adverse reaction

    Dist. by: Vi-Jon, LLC

    St. Louis, MO 63114

    www.germx.com

  • Disclaimer

    *Effective at eliminating 99.9% of many common harmful germs and bacteria in as little as 15 seconds.

    **Compare to ingredients in Germ-X Original Hand Sanitizer.

  • principal panel display

    germ-x ®

    SINCE 1997

    NOURISH

    MOISTURIZING HAND SANITIZER

    KILLS 99.9% OF GERMS

    6X

    MOISTURIZING INGREDIENTS

    with aloe & shea butter

    8FL OZ (236 ML)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-815
    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)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%) (UNII: 2N8MDB79NA)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-815-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/29/2024
    2NDC:83986-815-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/29/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/29/2024
    Labeler - UpLift Brands, LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-815)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-815)
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