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Ultra Seal Bacitracin (Ultra Seal Corporation)

Available Formats

Dosage Form Package Information Links
OINTMENT 1 TUBE in 1 CARTON (42213-400-28) > 28 g in 1 TUBE Label Information

Complete Ultra Seal Bacitracin Information

  • ACTIVE INGREDIENT

    In Each Gram-Bacitracin Zinc 500 units


  • PURPOSE

    Purpose: First Aid Antibiotic


  • INDICATIONS & USAGE

     First Aid to help prevent infection in minor cuts, burns, scrapes


  • WARNINGS

    DO NOT USE:  In the eyes.  Over large areas of the body. If you are allergic to any of the ingredients due to the possibility of anaphylactic shock. Longer than 1 week unless directed by a doctor.

    Stop use and ask a doctor before use: in the case of dep puncture wounds, animal bites, or serious burns.  If the condition persists or gets worse. If a rash or other allergic reaction develops.

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




  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children


  • DOSAGE & ADMINISTRATION

     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 1-3 times daily

    May be covered with a sterile bandage.


  • INACTIVE INGREDIENT

    inactive Ingredient: White Petrolatum


  • INGREDIENTS AND APPEARANCE
    ULTRA SEAL BACITRACIN  
    bacitracin zinc ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:42213-400
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [iU]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:42213-400-28 1 in 1 CARTON 12/04/2011
    1 28 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 12/04/2011
    Labeler - Ultra Seal Corporation (085752004)
    Registrant - ULTRAtab Laboratories, Inc. (151051757)
    Establishment
    Name Address ID/FEI Business Operations
    ULTRAtab Laboratories, Inc. 151051757 manufacture(42213-400)