Label: ALCOHOL liquid

  • NDC Code(s): 11673-988-16, 11673-988-34, 11673-988-45
  • Packager: Target
  • 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 March 15, 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 exterenal 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 thoroghly 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 105⁰F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, carbomer and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

  • SPL UNCLASSIFIED SECTION

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

    Dist. by Target Corp., Mpls., MN 55403

    Made in U.S.A. with U.S. and foreign components

    TM & (c)2023 Target Brands, Inc. 

    Guest Services 1-800-910-6874

  • principal display panel

    kills 99.99% of germs*

    hand

    sanitizer

    up & up

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-988
    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)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-988-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/29/2020
    2NDC:11673-988-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/29/2020
    3NDC:11673-988-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/29/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/29/2020
    Labeler - Target (006961700)
    Registrant - Vi Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC088520668manufacture(11673-988)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, LLC790752542manufacture(11673-988)
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