Label: EO HAND SANITIZER PEPPERMINT- alcohol spray

  • NDC Code(s): 54748-102-01, 54748-102-02, 54748-102-05, 54748-102-09, view more
    54748-102-12
  • Packager: EO Products, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 10, 2024

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  • Active Ingredients:

    Organic Ethanol 62%

  • Purpose:

    Antiseptic

  • Uses:

    • For hand washing to decrease bacteria on skin
    • Recommended for repeated use
  • Warnings:

    • Flammable, keep away from fire/flame
    • For external use only
    • Do not use in eyes. If contact occurs, flush thoroughly with water.
    • Stop use and ask a doctor if redness and irritation develop and persists for more than 72 hours.
  • KEEP OUT OF REACH OF CHILDREN

    • Keep out of reach of children. If swallowed, get medical help or contact the Poison Control center right away.
  • Directions:

    • Wet hands thoroughly with product and allow to dry without wiping.
    • Do not use other than intended.
  • Other Information:

    • Store below 104°F (40°C).
    • May discolor certain fabrics.
  • Inactive Ingredients:

    Purified Water, Organic Mentha Piperita (Peppermint) Oil, Organic Thymus Vulgaris (Thyme) Leaf Extract, Vegetable Glycerin, Tocopherol

  • SPL UNCLASSIFIED SECTION

    ESSENTIAL OILS

    USDA ORGANIC

    HAND sanitizer SPRAY

    peppermint

    99.9% EFFECTIVE AGAINST MOST COMMON GERMS
    made with moisturizing ingredients

    SYNTHETIC FRAGRANCE FREE

    TRICLOSAN FREE • BENZALKONIUM CHLORIDE FREE
    MADE WITH ORGANIC INGREDIENTS • PHTHALATE FREE

    EO® PRODUCTS
    SMALL WORLD TRADING CO. SAN RAFAEL, CA 94901
    MADE IN THE USA FROM DOMESTIC AND GLOBALLY SOURCED INGREDIENTS
    800-570-3775 eoproducts.com
    CERTIFIED ORGANIC BY CCOF

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    EO HAND SANITIZER  PEPPERMINT
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54748-102
    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)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    THYMUS VULGARIS LEAF (UNII: GRX3499643)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54748-102-0110 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/15/2013
    2NDC:54748-102-1212 in 1 BOX08/13/2018
    2NDC:54748-102-0110 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    3NDC:54748-102-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/15/201311/30/2016
    4NDC:54748-102-0559 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/02/2017
    5NDC:54748-102-096 in 1 BOX08/13/2018
    5NDC:54748-102-0559 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/15/2013
    Labeler - EO Products, LLC (786611210)
    Establishment
    NameAddressID/FEIBusiness Operations
    EO Products, LLC786611210manufacture(54748-102)
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