Label: ADVANCED HAND SANITIZER liquid

  • NDC Code(s): 83324-065-02, 83324-065-08
  • Packager: Chain Drug Marketing Association
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 19, 2026

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  • Active ingredient

    Ethyl alcohol 70% {v/v}

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

  • Disclaimer

    *This product is not manufactured or distributed by GOJO Industries, Inc., distributor of Purell ®Advanced Hand Sanitizer.

  • Claims

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

  • Adverse Reaction

    100% QC SATISFACTION GUARANTEED

    Distributed by CDMA, Inc.

    Novi, MI 48375

    www.qualitychoice.com

    Questions: 800-935-2362

  • Principal Display Panel

    NDC 83324-065-02

    QC ®

    QUALITY CHOICE

    Compare to Purell ®Advanced Hand Sanitizer*

    Advanced Hand Sanitizer

    Original

    Kills More Than 99.99% of Germs**

    Leaves Hands Feeling Soft

    With Moisturizers & Vitamin E

    2 FL OZ (59 mL)

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    ADVANCED HAND SANITIZER 
    advanced hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83324-065
    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 MONOCAPRYLOCAPRATE (UNII: G7515SW10N)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER (UNII: 0A5MM307FC)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83324-065-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/19/2026
    2NDC:83324-065-0259 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/19/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/19/2026
    Labeler - Chain Drug Marketing Association (011920774)
    Registrant - Nice-Pak Products, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091520manufacture(83324-065)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091514manufacture(83324-065)
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