Label: CHEMCOR CHEMICAL FOAMING HAND SANITIZER- benzalkonium chloride liquid

  • NDC Code(s): 68041-519-00, 68041-519-01
  • Packager: Chemcor Chemical Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated December 14, 2023

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  • Active Ingredient

    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 or 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
    • Rub hands together briskly until dry
  • Inactive Ingredients

    Water, Cocamidopropyl PG-dimonium Chloride Phosphate, Dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid.

  • SPL UNCLASSIFIED SECTION

    no alcohol

    dye and fragrance free

    tough on germs and bacteria

    CHEMCOR

    CHEMICAL CORP

    CHINO, CA 91710

    CHEMCORCHEMICAL.COM

    WARNING

    KEEP OUT OF REACH OF CHILDREN.

    MAY BE HARMFUL IF SWALLOWED.

    MAY CAUSE EYE IRRITATION.

    SEE BACK PANEL FOR ADDITIONAL PRECAUTIONS AND FIRST AID.

    institutional & commercial hand Sanitizer

    Before discarding container, rinse with water.

    For institutional and commercial use.

  • Foaming Hand Sanitizer

    image description
  • INGREDIENTS AND APPEARANCE
    CHEMCOR CHEMICAL FOAMING HAND SANITIZER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68041-519
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0013 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68041-519-004 in 1 BOX06/01/2020
    1NDC:68041-519-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/2020
    Labeler - Chemcor Chemical Corporation (018129978)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc.028311595manufacture(68041-519) , api manufacture(68041-519) , pack(68041-519)
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