Label: ALCOHOL liquid

  • 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 February 16, 2023

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  • Active ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Use

    • 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, fragrance, glycerin, isopropyl myristate, blue 1

  • Questions?

    Satisfaction quaranteed - For questions or comments please call 1-888-287-1915

  • SPL UNCLASSIFIED SECTION

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

    DISTRIBUTED BUY

    MEIJER DISTRIBUTION, INC.,

    GRAND RAPIDS, MI 49544

    471.000/471AA

  • principal display pane

    Meijer Hand Sanitizer

    Coastal Breeze

    kills 99.99% of germs*

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79481-9471
    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)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79481-9471-159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/03/2020
    2NDC:79481-9471-2236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/03/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/10/2019
    Labeler - MEIJER (006959555)
    Registrant - Vi Jon, Inc. (088520668)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, Inc.088520668manufacture(79481-9471)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi Jon, Inc.790752542manufacture(79481-9471)
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