Label: BZK ANTISEPTIC TOWELETTE- benzalkonium chloride solution

  • NDC Code(s): 60913-060-01
  • Packager: PHOENIX HEALTHCARE SOLUTIONS, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

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  • Active ingredient

    Benzalkonium Chloride, 0.13% v/v

  • Purpose

    Antiseptic

  • Uses

    • First aid antiseptic to help prevent skin infection in: minor cuts, scrapes and burns
    • Antiseptic Cleansing
    • Perineal and maternity care
  • Warnings:

    For external use only

    Do not

    • As an antiseptic for more than 1 week
    • In the eyes
    • Over large areas of the body

    Ask a doctor before use if you have

    • Deep or puncture wounds
    • Animal bites
    • Serious burns

    Stop use

    • If irritation and redness develop
    • If condition persists more than 72 hours, consult a physician.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    • Tear at notch
    • Remove towelette
    • Use only once

    As a first aid antiseptic:

    • Clean affected area
    • Apply 1 to 3 times daily
    • May be covered with a sterile bandage
    • If bandaged, let dry first
  • Other information

    • Store at room temperature
    • Avoid excessive heat
  • Inactive ingredients:

    Water

  • Principal Display Panel

    NDC 60913-060-01

    Phoenix Healthcare Solutions LLC

    "An Innovative Medical Manufacturer"

    BZK Antiseptic Towelette

    Contains Benzalkonium Chloride

    For Individual, Professional and Hospital Use

    100 Pouches Per Box

    1 Towelette Per Pouch

    Label

  • INGREDIENTS AND APPEARANCE
    BZK ANTISEPTIC  TOWELETTE
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60913-060
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60913-060-01100 in 1 BOX07/01/2015
    11 in 1 POUCH
    11.3 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/01/2015
    Labeler - PHOENIX HEALTHCARE SOLUTIONS, LLC (079146847)
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