Label: BACITRACIN ointment

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

Drug Label Information

Updated September 23, 2024

If you are a consumer or patient please visit this version.

  • 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. (1-800-222-1222)

  • 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?

    1-800-632-6900

  • Principal Display Panel

    Bacitracin Ointment, USP

    First Aid Antibiotic Ointment

    Helps prevent infection in minor cuts, scrapes & burns

    NET WT 1.0 OZ (28g)

    bacitracin image
  • INGREDIENTS AND APPEARANCE
    BACITRACIN 
    bacitracin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:30142-536
    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:30142-536-641 in 1 CARTON04/19/2017
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00404/19/2017
    Labeler - Kroger Company (006999528)