Label: HAND SANITIZING WIPES- benzalkonium chloride cloth

  • NDC Code(s): 69446-220-00
  • Packager: Ez Products Of South Florida, LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 23, 2023

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride (BZK) 0.1%

    Purpose

    Antibacterial

  • Use

    • Decrease bacteria on the skin.
  • Warnings

    For external use only.

    When using this product

    avoid contact with eyes.If contact occurs, rinse thoroughly with water.

    Do not use

    if irritation and redness develop.

    Stop use and seek medical attention

    if condition persists for more than 72 hours.

    Keep out of reach of children.

    If swallowed, seek medical attention or contact Poison Control Center.

  • DIRECTIONS

    1. Locate tear-notch on the side of pouch. 2. Tear straight across to open.  3. Pull first wipe from center of roll and thread wipe through dispensing nozzle

    Do not remove wipes roll from pouch.

  • Other information

    • Dispose of wipe in the proper container.
    • Do not flush down the toilet.
  • Inactive ingredients

    2-Bromo-2-Nitropropane-1,3-Diol, Alcohol,Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Fragrance, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA, Water.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69446-220
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BRONOPOL (UNII: 6PU1E16C9W)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69446-220-001500 in 1 BAG04/30/2021
    12.346 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/30/2021
    Labeler - Ez Products Of South Florida, LLC (113456060)
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