Label: LITE NFOAMY EUCALYPTUS MINT SANITIZING HANDWASH- benzalkonium chloride soap

  • NDC Code(s): 64009-332-72, 64009-332-75, 64009-332-78
  • Packager: Spartan Chemical Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 19, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients

    Benzalkonium Chloride 0.13%

  • Purpose

    Antimicrobial

  • Uses

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

    • For external use only

    When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if irritation and redness develops, or if 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

    • Pump a small amount of foam into palm of hand.
    • Rub thoroughly over all surfaces of both hands for 15 seconds.
    • Rinse with potable water.
  • Inactive Ingredients

    Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance

  • Questions?

    1-800-537-8990

  • Principal Display Panel - Container Label

    Spartan®

    Lite'nFoamy®

    Eucalyptus Mint

    Sanitizing Handwash

    Foam Sanitizing Handwash with Fragrance

    • For hand washing to decrease bacteria on the skin
    • Meets the hand care needs of institutional and industrial personnel

    FOR INSTITUTIONAL AND INDUSTRIAL USE ONLY

    See back panel for additional information.

    Manufactured by

    Spartan Chemical Company, Inc. 1110 Spartan Drive, Maumee, OH 43537 USA

    Medical Emergency: 888-314-6171 / www.spartanchemical.com

    Net Contents: 1 U.S. Gallon / 3.79 Liters

    EucMint Gal V02

  • INGREDIENTS AND APPEARANCE
    LITE NFOAMY EUCALYPTUS MINT SANITIZING HANDWASH 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64009-332
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64009-332-753.79 L in 1 CONTAINER; Type 0: Not a Combination Product04/14/2014
    2NDC:64009-332-78280.2 L in 1 CONTAINER; Type 0: Not a Combination Product04/14/2014
    3NDC:64009-332-720.532 L in 1 CONTAINER; Type 0: Not a Combination Product04/14/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/14/2014
    Labeler - Spartan Chemical Company (005036728)
    Establishment
    NameAddressID/FEIBusiness Operations
    Spartan Chemical Company005036728manufacture(64009-332)
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