Label: ADVANCED HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 83986-439-16, 83986-439-32, 83986-439-34, 83986-439-50, view more
    83986-439-86
  • Packager: UpLift Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 23, 2024

If you are a consumer or patient please visit this version.

  • 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 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
    • conditon 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, Aloe barbadensis leaf juice, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4, blue 1, yellow 5

  • Disclaimer

    DSP-TN-21091 DSP-MO-20087 DSP-MO-28 SDS-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 

    EMPLOYY-OWNED

  • Advrse 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 WITH ALOE

    Kills more than 99.99% of Germs*

    with added moisturizers

    33.8 FL OZ (1L) 1.05 QT

    image description

  • INGREDIENTS AND APPEARANCE
    ADVANCED HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-439
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-439-1659 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/23/2024
    2NDC:83986-439-34236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/23/2024
    3NDC:83986-439-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/23/2024
    4NDC:83986-439-32355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/23/2024
    5NDC:83986-439-50709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/23/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/23/2024
    Labeler - UpLift Brands LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-439)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-439)