Label: KIMBALL MIDWEST ANTIBACTERIAL HAND CLEANER- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2024

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  • Drug Facts

  • Active Ingredient

    Benzalkonium Chloride 0.13% w/v

  • Purpose

    Antibacterial Agent

  • Uses

    To decrease bacteria on the skin.

  • Warnings

    For external use only.

    Avoid contact with eyes. If contact occurs, flush eyes with water. 

    Stop use and ask a doctor if, in rare instances, redness or irritation develops and persists for more than 72 hours.

    Keep out of reach of children. If swallowed, contact a physician or poison control center.

  • Directions

    Apply small amount, covering hands with product for 30 seconds. Add water, lather, rinse.

  • Inactive Ingredients

    Water, Cetrimonium Chloride, Lauramine Oxide, Sorbitol, Cocamide MEA, Sodium Chloride, PEG-120 Methyl Glucose Dioleate, Sodium Lauraminodipropionate, Citric Acid, Fragrance, Disodium EDTA, Methylisothiazolinone, Methychloroisothiazolinone, Yellow 5, Red 33.

  • SPL UNCLASSIFIED SECTION

    Proven To Kill A Broad Spectrum Of Germs And Bacteria

    Mild Yet Effective

    Pleasant Spicy Floral Fragrance

    Carefully read warnings on side panel

    FOR INDUSTRIAL AND PROFESSIONAL USE ONLY

    Manufactured for:
    Kimball Midwest
    4800 Roberts Rd.
    Columbus, Ohio 43228
    800-233-1294
    www.kimballmidwest.com

    DESCRIPTION
    The Antibacterial Hand Cleaner is a fast-acting hand cleaner with a pleasant spicy floral fragrance. Kill germs without irritating the skin and helps prevent drying, cracking and chapping.

    DIRECTIONS
    Apply Antibacterial Hand Cleaner to wet hands. Work thoroughly into hands, knuckles and under fingernails. Rinse with water.

    Made in the U.S.A.

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    KIMBALL MIDWEST ANTIBACTERIAL HAND CLEANER 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66608-216
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SORBITOL (UNII: 506T60A25R)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    SODIUM LAURIMINODIPROPIONATE (UNII: 7G447D0DH9)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66608-216-013785 mL in 1 BOTTLE; Type 0: Not a Combination Product11/13/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/13/2024
    Labeler - Kimball Midwest (017906231)
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