Label: ADVANCED HAND SANITIZER- alcohol gel

  • NDC Code(s): 63868-882-16, 63868-882-34, 63868-882-43, 63868-882-45
  • Packager: CDMA
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 27, 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 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 of children.

    If swallowed get medical help or contact a Poison Control Center right away.

  • Directions

    • wet hands thoroghly 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 sore above 105⁰ F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

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

  • SPL UNCLASSIFIED SECTION

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

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

    Distributed by CDMA, Inc.

    43157 W Nine Mile

    Novi, MI 48357

    www.qualitychoice.com

    Questions: 800-935-2362

  • principal display panel

    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 description

  • INGREDIENTS AND APPEARANCE
    ADVANCED HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-882
    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 COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-882-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
    2NDC:63868-882-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
    3NDC:63868-882-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
    4NDC:63868-882-43473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/05/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/05/2021
    Labeler - CDMA (011920774)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(63868-882)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(63868-882)
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