Label: FIRST AID ANTIBIOTIC- bacitracin zinc ointment

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

Drug Label Information

Updated January 17, 2024

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  • Drug Facts

  • Active Ingredient

    Bacitracin 500 units 

  • Uses

    Bacitracin -First Aid Antibiotic 

  • Uses

    First aid to help prevent infection in minor:

    • cuts
    • scrapes
    • burns
  • Warnings

    For external use only 

    Allergy alert do not use if you are allergic to any of the ingredients 

    Do not use

    • in or near eyes
    • on large arteas of the body 

    Consult a doctor before use if you have

    • deep puncture wounds 
    • animal bites
    • serious burns 

    When using this product

    • do not use longer than 1 week 
  • Stop use and consult a doctor if 

    • condition persists or gets worse
    • symptoms last for more than 7 days or clear up and come back within a few days
    • a rash or other allergic reaction develops
  • Keep out of the reach of children

    If swallowed get medical help or contact a Poison Control Center immediately.

  • Directions

    • clean the affected area
    • apply a small amount (equal to surface area of tip of finger) on the area 1 to 3 times daily.
    • may be covered with a sterile bandage
  • Other information 

    Store at a controlled room temperature 20º-25ºC (68° to 77°F)

  • Inactive ingredient 

    Petrolatum 

  • Questions? 1-800-910-6874

  • Principal Display Panel 

    Target Up and Up       NDC 11673-790-14

    Bacitracin ointment

    First aid Antibiotic Ointment 

    NET WT 0.5OZ (14g)

    291020 Tube

    591020 Carton

  • INGREDIENTS AND APPEARANCE
    FIRST AID ANTIBIOTIC 
    bacitracin zinc ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-790
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-790-141 in 1 CARTON01/31/2024
    114 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00401/31/2024
    Labeler - Target Corporation (006961700)
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