Label: ETHYL ALCOHOL gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 22, 2023

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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 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 ot inhale or ingest
  • Stop use and ask a doctor if

    • irritation and redness develop
    • condiion persists for more than 72 hours
  • Keep out of the 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 105°F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, glycerin, propylene glycol, fragrance, acrylates/C10-30 alkyl acrylate crosspolymer, triethanolamine, blue 1, red 40, yellow 5

  • Adverse Reactions

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

    DISTRIBUTED BY: Walmart, Inc., Bentonville, AR 72716

    Product of China

  • Principal Panel Display

    NDC 49035-418-10

    equate

    HAND

    SANITIZER

    Sandalwood & Sea

    Kills 99.99% of Germs

    Contains

    Moisturizers

    1 FL OZ (29.5 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ETHYL ALCOHOL 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-418
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-418-1029.5 mL in 1 PACKAGE; Type 0: Not a Combination Product12/03/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/03/2019
    Labeler - Wal-Mart Stores, Inc. (051957769)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nantong Health & Beyond Hygenic Products, Inc.421280161manufacture(49035-418)
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