Label: ANTISEPTIC WIPE- benzalkonium chloride solution

  • NDC Code(s): 72459-281-00
  • Packager: Yiwu Ori-Power Medtech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 18, 2024

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  • DRUG FACTS

  • Active Ingredients

    Benzalkonium Chloride 0.13%

    Purpose

    First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

  • Inactive Ingredients

    Purfied water, Sodium Bicarbonate

  • Use

    Sanitize hands Clean wounds

  • Directions

    Tear open packet, unfold towelette, use to cleanse desired skin area. Discard towelette appropriately after use.

  • Storage

    Store at room temperature 15°C - 30°C (59°F - 86°F).

  • Warnings

    Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If pain, irritation, redness, swelling, or infection develops, discontinue use and consult physician.

    Keep Out Of Reach Of Children

    In case of accidental swallowing, seek medical help and contact poison control imeediately

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC WIPE 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72459-281
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72459-281-001.6 g in 1 POUCH; Type 0: Not a Combination Product02/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/01/2024
    Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)
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