Label: KROGER ANTIBACTERIAL- benzalkonium chloride liquid

  • NDC Code(s): 41226-500-11, 41226-500-52
  • Packager: Kroger Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 24, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    Helps decrease bacteria on hands

  • Warnings

    For external use only

    When using this product

    Avoid contact with eyes. In case of contact, flush 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, seek medical attention or contact a Poison Control Center immediately.

  • Directions

    • From Pump bottle, apply onto wet hands
    • Lather and rinse thoroughly.
  • Other Information

    Store at room Temperature.

  • Inactive Ingredients

    Water (Aqua), Lauramidopropylamine Oxide, Glycerin, Cetrimonium Chloride, Sodium Chloride, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Fragrance (Parfum), Citric Acid, Tetrasodium EDTA, Sodium Sulfate, Methylchloroisothiazolinone, Meisothiazolinone, Yellow 5 (CI 19140), Red 4 (CI 17400).

  • PDP- 41226-500-11 (325 ml)

    325 ml

  • PDP-2, NDC- 41226-500-52

    Principal Display Panel-2

  • INGREDIENTS AND APPEARANCE
    KROGER ANTIBACTERIAL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41226-500
    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
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41226-500-11325 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/05/2024
    2NDC:41226-500-521538 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/05/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/05/2024
    Labeler - Kroger Company (006999528)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(41226-500)
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