Label: THOMPSON ANTISEPTIC- benzalkonium chloride swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 8, 2023

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  • Drug Facts

  • ACTIVE INGREDIENT

    Benzalkonium chloride 0.133% w/v

  • PURPOSE

    First aid antiseptic

  • INDICATIONS & USAGE

    First aid to help prevent infection in minor cuts, scrapes and burns.

  • WARNINGS

    in the eyes or over large areas of the body
    in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
    longer than 1 week unless directed by a doctor

  • DO NOT USE

    in the eyes or over large areas of the body
    in case of deep or puncture wounds, animal bites or serious burns, consult a doctor
    longer than 1 week unless directed by a doctor

  • STOP USE

    the condition persists or gets worse

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    tear open packet, unfold and celan the affected area
    discard after use
    may be covered with a sterile bandage
    if bandaged, let dry first

  • OTHER SAFETY INFORMATION

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

    tamper evident sealed packets

    do not use any open or torn packets

  • INACTIVE INGREDIENT

    sodium bicarbonate, water

  • QUESTIONS

    1.877.506.4291

  • PRINCIPAL DISPLAY PANEL

    Antiseptic Wipes

    Benzalonium Chloride 0.133% W/V

    FIRST AID ANTISEPTIC

    FIRST AID TO HELP PREVENT INFECTION IN MINOR CUTS, SCRAPES AND BURNS

    50/Box

    THOMPSON
    SAFETY WORKS BUSINESS THRIVES ᵀᴹ

    CS103050 Antiseptic wipes

  • INGREDIENTS AND APPEARANCE
    THOMPSON ANTISEPTIC 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73408-034
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73408-034-5050 in 1 BOX12/05/2023
    11.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/05/2023
    Labeler - Thompson (080998015)
    Registrant - UniFirst First Aid Coproation (832947092)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America874965262manufacture(73408-034)
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