Label: HAND SANITIZER- alcohol gel

  • NDC Code(s): 83986-456-04, 83986-456-44, 83986-456-45, 83986-456-86
  • Packager: UpLift Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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  • Active ingredient

    Ethyl alcohol 70%

  • Purpose

    Antiseptic

  • Use

    • 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 or redness develops
    • condition persists for more than 72 hours
  • Keep out of reach 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 suervision
    • not recommended for infants
  • Other information

    • do not store above 105° F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, PEG-8 Dimethicone, meadowfoamamidopropyl betaine, glyceryl caprylate/caprate, glycerin, tocopheryl acetate, isopropyl myristate

  • Claims

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

  • Adverse reaction

    DISTRIBUTED BY: VI-JON, INC.

    8515 Page Ave

    ST. LOUIS, MO 63114

    vijonprofessional.com

  • Principal display panel

    germ-x ®

    Professional

    ADVANCED FOAMING HAND SANITIZER

    Kills 99.99% of Germs*

    Fragrance Free

    Dye Free

    18 FL OZ (532 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-456
    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)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-456-451150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/2024
    2NDC:83986-456-04750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/2024
    3NDC:83986-456-44532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/2024
    4NDC:83986-456-861000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/15/2024
    Labeler - UpLift Brands, LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-456)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(83986-456)
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