Label: ANTIBACTERIAL LHS- benzalkonium chloride liquid

  • NDC Code(s): 82442-004-07
  • Packager: TARGET CORPORATION INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 19, 2024

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  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    helps eliminate bacteria on hands.

  • Warnings

    For external use only

    When using this product

    • Avoid contact with eyes. In case of contact, rinse thoroughly with water.

    Stop use and ask a doctor if

    • irritation or redness develops and lasts.

    Keep out of reach of children.

    In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

  • Directions

    • From Liquid Hand Soap pump bottle, apply onto wet hands.
    • Lather and rinse thoroughly.
  • Inactive ingredients

    Water (Aqua), Cocamidopropyl Betaine, Hydroxyethylcellulose, Glycerin, Poloxamer 124, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Red 40 (CI 16035), Red 33 (CI 17200), Yellow 5 (CI 19140).

  • Questions

    1-800-910-6874

  • Principal Display Panel

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL LHS 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE130 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    POLOXAMER 124 (UNII: 1S66E28KXA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-004-07222 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/01/2024
    Labeler - TARGET CORPORATION INC. (006961700)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(82442-004)
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