Label: EO HAND SANITIZER SWEET ORANGE- alcohol spray

  • NDC Code(s): 54748-103-02, 54748-103-05, 54748-103-09
  • 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 Lavandula Angustifolia (Lavender) Oil, Organic Citrus Aurantium Dulcis (Orange) Peel Oil, Organic Citrus Medica Limonum (Lemon) Peel Oil, Vegetable Glycerin, Tocopherol

  • SPL UNCLASSIFIED SECTION

    ESSENTIAL OILS

    USDA ORGANIC

    HAND sanitizer SPRAY

    sweet orange

    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

    EOrange59

  • INGREDIENTS AND APPEARANCE
    EO HAND SANITIZER  SWEET ORANGE
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54748-103
    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)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LEMON OIL (UNII: I9GRO824LL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54748-103-0260 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/15/201311/30/2016
    2NDC:54748-103-0559 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/02/2017
    3NDC:54748-103-096 in 1 BOX08/13/2018
    3NDC:54748-103-0559 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(54748-103)
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