Label: HAND SANITIZER- alcohol gel

  • NDC Code(s): 83986-652-04, 83986-652-08, 83986-652-16, 83986-652-34, view more
    83986-652-45, 83986-652-48, 83986-652-55, 83986-652-68, 83986-652-86
  • Packager: UpLift Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 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 and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

  • Adverse Reaction

    DISTRIBUTED BY: UPLIFT BRANDS, LLC

    ST. LOUIS, MO 63114

    1-866 MY GERMX

    DSP-TN-21091

    DSP-MO-20087

  • Principal panel display

    germ-X ®

    PRO

    MOISTURIZING

    HAND SANITIZER

    750 mL (1.58 PT) 25.4 FL OZ

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-652
    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:83986-652-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    2NDC:83986-652-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    3NDC:83986-652-04750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    4NDC:83986-652-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    5NDC:83986-652-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    6NDC:83986-652-481150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    7NDC:83986-652-682000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    8NDC:83986-652-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2022
    9NDC:83986-652-552082 mL in 1 DRUM; Type 0: Not a Combination Product12/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/06/2022
    Labeler - UpLift Brands, LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-652)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-652)
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