Label: THOMPSON ANTISEPTIC- benzalkonium chloride swab

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

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 February 21, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium chloride 0.33% w/v

  • PURPOSE

    Purpose

    First aid antiseptic

  • INDICATIONS & USAGE

    Uses

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

  • WARNINGS

    Warnings

  • DO NOT USE

    Do not use

    • in the eyes or apply over larger area of the body
    • in case of deep puncture wounds, aniamal bites or serious burns, consult a doctor
    • longer than 1 week unless directed by a doctor
  • STOP USE

    Stop use and ask a doctor if

    • the condition persists or gets worse
  • 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.

  • DOSAGE & ADMINISTRATION

    Directions

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

    Other information

    • store at room temperature 59º-86ºF (15º-30ºC)
    • tamper evident sealed packets
    • do not use any open or torn packets
  • INACTIVE INGREDIENT

    Inactive ingredients sodium bicarbonate, water

  • QUESTIONS

    Questions or comments? 1.877.506.4291

  • PRINCIPAL DISPLAY PANEL

    Antiseptic Wipes

    Benzalkonium Chloride 0.133% w/v

    First Aid Antiseptic

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

    20/Box

    Thompson

    Safety Works | Business Thrives™

    CS103071

  • INGREDIENTS AND APPEARANCE
    THOMPSON ANTISEPTIC 
    benzalkonium chloride swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73408-032
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.33 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73408-032-7120 in 1 BOX05/01/2023
    11.4 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/01/2023
    Labeler - Thompson (080998015)
    Registrant - Unifirst First Aid Corporation (832947092)
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