Label: EO HAND SANITIZER LAVENDER- alcohol gel

  • NDC Code(s): 54748-201-02, 54748-201-03, 54748-201-04, 54748-201-05, view more
    54748-201-07, 54748-201-08, 54748-201-09, 54748-201-17
  • Packager: EO Products, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 11, 2024

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  • 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 or flame.
    • For external use only.
    • Do not use in eyes. If contact occurs, flush thoroughly with water.
    • Stop use and ask doctor if redness and irritation develops and persists for more than 72 hours.

    • 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.

  • Other Information:

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

    Purified Water, Vegetable Glycerin, EO® Essential Oil Blend [Organic Lavandula Angustifolia (Lavender) Oil, Lavandula Hybrida Oil], Organic Simmondsia Chinensis (Jojoba) Seed Oil, Carbomer, Dimethicone, Aminomethyl Propanol

  • SPL UNCLASSIFIED SECTION

    ESSENTIAL OILS

    HAND sanitizer GEL

    french lavender

    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

  • Packaging

    54748-201

  • INGREDIENTS AND APPEARANCE
    EO HAND SANITIZER  LAVENDER
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54748-201
    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)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    JOJOBA OIL (UNII: 724GKU717M)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54748-201-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/201310/31/2016
    2NDC:54748-201-03240 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/201310/31/2016
    3NDC:54748-201-04960 mL in 1 BOTTLE; Type 0: Not a Combination Product01/15/201310/31/2016
    4NDC:54748-201-0559 mL in 1 BOTTLE; Type 0: Not a Combination Product05/02/2017
    5NDC:54748-201-096 in 1 BOX08/13/2018
    5NDC:54748-201-0559 mL in 1 BOTTLE; Type 0: Not a Combination Product
    6NDC:54748-201-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/15/2017
    7NDC:54748-201-07946 mL in 1 BOTTLE; Type 0: Not a Combination Product05/15/2017
    8NDC:54748-201-17946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/01/2022
    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(54748-201)
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