Label: LITE NFOAMY E3 HAND SANITIZER- benzalkonium chloride soap

  • NDC Code(s): 64009-334-05, 64009-334-08
  • 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 0.1%

  • Purpose

    Antimicrobial

  • Uses

    • For hand sanitizing 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

    • Hands must be washed and rinsed with potable water before use.
    • Pump a small amount of foam into palm of hand.
    • Rub thoroughly over all surfaces of both hands.
    • Rub hands together briskly until dry.
  • Other Information

    • This product must be dispensed from an adequate dispenser located a sufficient distance from processing line to prevent accidental product contamination.
    • Do not contaminate water, food or feed by storage and disposal.
  • Inactive Ingredients

    Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxethyl Cocamine Oxide, Glycereth-17-Cocoate, Citric Acid

  • Questions?

    1 -800-537-8990

  • Principal Display Panel - Container Label

    Lite n Foamy E3 Hand Sanitizer Gallon

  • INGREDIENTS AND APPEARANCE
    LITE NFOAMY E3 HAND SANITIZER 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64009-334
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64009-334-053.79 L in 1 CONTAINER; Type 0: Not a Combination Product04/01/2014
    2NDC:64009-334-08280.2 L in 1 CONTAINER; Type 0: Not a Combination Product04/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/01/2014
    Labeler - Spartan Chemical Company (005036728)
    Establishment
    NameAddressID/FEIBusiness Operations
    Spartan Chemical Company005036728manufacture(64009-334)
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