Label: MEDICHOICE OB CLEANSING- benzalkonium chloride cloth

  • NDC Code(s): 39892-0306-1
  • Packager: Owens & Minor Distribution, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 9, 2023

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  • Drug Facts

  • Active ingredient

    Benzalkonium Chloride, 0.13% w/w

    Purpose

    First Aid Antiseptic

  • Use

    First aid antiseptic product to apply topically to the skin to help prevent infection in minor cuts, scrapes, and burns.

  • Warnings

    For external use only. Do not insert into the vagina. 

    Do not use 

    • in the eyes or apply over large areas of the body.
    • longer than 1 week unless directed by a doctor. 
    • no infants.  Consult a doctor
    • in case of deep or punture wounds, animal bites, or serious burns.

    Stop use and consult a doctor

    If 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.

  • Directions

    • Clean the affected area 1 to 3 times daily or as directed by a doctor. May be covered with a sterile bandage when dry.
  • Other information

    • Store at room temperature.
    • Allow pad to air dry before disposal.
  • Inactive ingredient

    Isopropyl Alcohol, Purified Water, Thyme Camphor

  • Package Labeling:

    Label3Box2

  • INGREDIENTS AND APPEARANCE
    MEDICHOICE OB CLEANSING 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0306
    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
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    THYMOL (UNII: 3J50XA376E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:39892-0306-110 in 1 CASE08/29/2017
    1100 in 1 BOX
    11 in 1 PACKET
    10.75 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/29/2017
    Labeler - Owens & Minor Distribution, Inc. (847412269)
    Registrant - Owens & Minor Distribution, Inc. (847412269)
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