Label: BACITRACIN ointment

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

Drug Label Information

Updated April 30, 2024

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  • Active ingredient (each gram contains)

    Bacitracin 500 units

  • Purpose

    First aid antibiotic

  • Uses

    first aid to help prevent infection in:

    •
    minor cuts
    •
    scrapes
    •
    burns
  • Warnings

    For external use only

    Do not use

    •
    in the eyes
    •
    over large areas of the body
    •
    if you are allergic to any of the ingredients

    Ask a doctor before use if you have

    •
    deep or puncture wounds
    •
    animal bites
    •
    serious burns

    Stop use and ask a doctor if

    •
    you need to use longer than 1 week
    •
    condition persists or gets worse
    •
    rash or other allergic reaction develops

    Keep out of reach of children.

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

  • Directions

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

    •
    store at 20°-25°C (68°-77°F)
  • Inactive ingredients

    light mineral oil, white petrolatum

  • Questions or comments?

    1-800-719-9260

  • HOW SUPPLIED

    Bacitracin First Aid Antibiotic Ointment

    • NDC 72162-2280-2: 144 Unit dose 

    Repackaged/Relabeled by:
    Bryant Ranch Prepack, Inc.
    Burbank, CA 91504

  • PRINCIPAL DISPLAY PANEL

    Bacitracin First Aid Antibiotic Ointment 

    144 Unit Dose 

    NET WT 0.9 g Each

    Label
  • INGREDIENTS AND APPEARANCE
    BACITRACIN 
    bacitracin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72162-2280(NDC:45802-060)
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72162-2280-2144 in 1 CARTON04/30/2024
    10.9 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00406/20/2011
    Labeler - Bryant Ranch Prepack (171714327)
    Registrant - Bryant Ranch Prepack (171714327)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bryant Ranch Prepack171714327REPACK(72162-2280) , RELABEL(72162-2280)
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