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Bacitracin (Preferred Pharmaceuticals, Inc)

Available Formats

Dosage Form Package Information Links
OINTMENT 14 g in 1 TUBE (68788-9794-1) Label Information
OINTMENT 28 g in 1 TUBE (68788-9794-2) Label Information

Complete Bacitracin Information

  • ACTIVE INGREDIENT

    Bacitracin 500 units


  • PURPOSE

    First aid antibiotic


  • USES

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


  • WARNINGS

    For external use only
    Do not use
    if you are allergic to any of the ingredients
    in the eyes
    over large areas of the body
    longer than 1 week unless directed by a doctor

    Ask a doctor before use in case of deep or puncture wounds, animal bites, or serious burns

    Stop use and ask a doctor if
    the condition persists or gets worse
    a 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 room temperature


  • INACTIVE INGREDIENT

    light mineral oil, white petrolatum


  • HOW SUPPLIED

    14gm tube – 68788-9794-1

    28gm tube – 68788-9794-2

    Relabeled By Preferred Pharmaceuticals, Inc


  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Bacitracin Ointment First Aid Antibiotic

  • INGREDIENTS AND APPEARANCE
    BACITRACIN 
    bacitracin ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:68788-9794(NDC:0713-0280)
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Bacitracin (UNII: 58H6RWO52I) (Bacitracin - UNII:58H6RWO52I) Bacitracin 500 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    Light Mineral Oil (UNII: N6K5787QVP)  
    Petrolatum (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:68788-9794-1 14 g in 1 TUBE; Type 0: Not a Combination Product 04/30/2012
    2 NDC:68788-9794-2 28 g in 1 TUBE; Type 0: Not a Combination Product 04/30/2012
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 04/30/2012
    Labeler - Preferred Pharmaceuticals, Inc (791119022)
    Registrant - Preferred Pharmaceuticals, Inc (791119022)
    Establishment
    Name Address ID/FEI Business Operations
    Preferred Pharmaceuticals, Inc 791119022 RELABEL(68788-9794)