Label: EVERYONE HAND SANITIZER PEPPERMINT CITRUS- alcohol gel

  • NDC Code(s): 54748-402-02, 54748-402-05, 54748-402-09
  • Packager: EO Products, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 10, 2024

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  • Drug Facts

  • Active Ingredients:

    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 contact a doctor if redness and irritation develops 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 directed.

  • Inactive Ingredients:

    Purified Water, Vegetable Glycerin, EO® Essential Oil Blend [Citrus Aurantium Dulcis (Orange) Peel Oil, Lavandula Angustifolia (Lavender) Oil, Mentha Piperita (Peppermint) Oil], Organic Simmondsia Chinensis (Jojoba) Seed Oil, Carbomer, Dimethicone, Aminomethyl Propanol, *Limonene

    *component of essential oil

  • Other Information:

    • Store at room temperature 20°-25°C (66°F - 77°F)
    • May discolor certain fabrics.
  • SPL UNCLASSIFIED SECTION

    99.9% EFFECTIVE against most common germs

    clean hands now

    no parabens / no synthetic fragrances / no triclosan

    made with moisturizing ingredients

    EO® PRODUCTS

    Small World Trading Co. San Rafael, CA 94901

    Made in the USA From Domestic and Globally Sourced Ingredients

    800-570-3775 www.eoproducts.com

  • Packaging

    Peppermint Citrus label

  • INGREDIENTS AND APPEARANCE
    EVERYONE HAND SANITIZER  PEPPERMINT CITRUS
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54748-402
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    JOJOBA OIL (UNII: 724GKU717M)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54748-402-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product06/07/201302/15/2017
    2NDC:54748-402-0559 mL in 1 BOTTLE; Type 0: Not a Combination Product08/31/2018
    3NDC:54748-402-096 in 1 PACKAGE08/31/2018
    3NDC:54748-402-0559 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/07/2013
    Labeler - EO Products, LLC (786611210)
    Establishment
    NameAddressID/FEIBusiness Operations
    EO Products, LLC786611210manufacture(54748-402)
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