Label: BZK PADS- benzalkonium chloride swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 01/14

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  • ACTIVE INGREDIENT

    Active Ingredient                                     Purpose

    Benzalkonium Chloride 0.13% v/v              Antiseptic

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  • Warnings

    For external use only

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  • Purpose

    Benzalkonium Chloride Cleansing

    First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns
    Antiseptic cleansing
    Perineal and maternity care

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  • Stop use if

    Stop Use if:

    • irritation and redness develop
    • if condition persists for more than 72 hours, consult a physician.
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  • Indications & Usage

    General antiseptic

    Ask a doctor before use if you have
    deep or puncture wounds
    animal bites
    serious burns

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  • Dosage & Administration

    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

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  • Keep out of reach of children


    Keep out of reach of children

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

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  • Do not use

    Do not use

    • as a first aid antiseptic for more than 1 week
    • in the eyes
    • over large areas of the body
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  • Inactive ingredient section

    Inactive ingredient(s): chlorothymal, ispropyl alcohol, water

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  • Principal display panel(s)

    Benzalkonium_Chloride_Cleansing.jpg

    Benzalkonium_Chloride_Cleansing

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  • INGREDIENTS AND APPEARANCE
    BZK PADS 
    benzalkonium chloride swab
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:67777-243
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:67777-243-01 .55 mL in 1 PACKET
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 04/05/2011
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
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