Label: CRANBERRY GARLAND- ethyl alcohol gel

  • NDC Code(s): 41250-122-16, 41250-122-34
  • Packager: Meijers Distribution, Inc
  • 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 17, 2022

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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 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 hand 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, carbomer, fragrance, red 33, blue 1

  • SPL UNCLASSIFIED SECTION

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

    DISTRIBUTED BY

    MEIJER DISTRIBUTION, INC.

    GRAND RAPIDS, MI 49544

    QUESTIONS 1-888-593-0593

  • principal display panel

    meijer

    Hand Sanitizer

    Cranberry Garland

    Kills 99.99% of germs

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    CRANBERRY GARLAND 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41250-122-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/24/2016
    2NDC:41250-122-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/24/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/24/2016
    Labeler - Meijers Distribution, Inc (006959555)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(41250-122)
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