Label: HAND SANITIZER- ethyl alcohol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 26, 2024

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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

    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 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

    • spray 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, Aloe barbadensis leaf juice, fragrance, limonene

  • Questions

    1-888-593-0593

  • Disclaimer

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

  • SPL UNCLASSIFIED SECTION

    Distributed By: Vi-Jon, LLC

    8515 Page AVe., St. Louis, MO 63114

    www.germx.com

    FORMULA MADE IN THE USA

    EMPLOYEE-OWNED

  • Principal display panel

    germ-X ®

    SINCE 1997

    KILLS 99.99% OF GERMS

    HAND SANITIZER SPRAY

    LAVENDER SCENT

    KILLS GERMS IN 15 SECONDS*

    FORMULA MADE IN USA ENPLOYEE-OWNED

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83986-721
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    LIMONENE OXIDE, (+)- (UNII: 278IM94GXB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83986-721-2059 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/26/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/26/2024
    Labeler - UpLift Brands, LLC (119091527)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(83986-721)
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