Label: HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 83986-529-16, 83986-529-32, 83986-529-34, 83986-529-50, view more
    83986-529-86
  • Packager: UpLift Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 20, 2024

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  • Active Ingredient

    Ethyl alcohol 70%

  • 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 heat and 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 develops
    • 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, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

  • Disclaimer

    DSP-TN-21091 DSP-MO-20087 DSP-MO-28 DSD-MO-20068

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

    FORMULA MADE IN USA

    EMPLOYEE OWNED

  • Adverse reaction

    Dist. by: Vi-Jon, LLC 8515 Page Ave

    St. Louis, MO 63114

  • Principal display panel

    germ-x®

    since 1997

    ADVANCED

    70% alcohol hand sanitizer

    Kills more than 99.99% of Germs*

    with added moisturizers

    33.8 FL OZ (1L) 1.05QT

    mm01

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-529
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-529-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/22/2022
    2NDC:83986-529-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/22/2022
    3NDC:83986-529-32355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/22/2022
    4NDC:83986-529-50710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/22/2022
    5NDC:83986-529-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/22/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM505G(a)(3)12/22/2022
    Labeler - UpLift Brands LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-529)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-529)
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