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ULTRA SEAL Triple Antibiotic (Ultra Seal Corporation)

Available Formats

Dosage Form Package Information Links
OINTMENT 1 TUBE in 1 CARTON (42213-360-28) > 28 g in 1 TUBE Label Information
OINTMENT 144 PACKET in 1 BOX (42213-360-80) > .9 g in 1 PACKET (42213-360-09) Label Information

Complete ULTRA SEAL Triple Antibiotic Information

  • ACTIVE INGREDIENT

    Actve Ingredients: In each gram-Neomycin Sulfate-5 mg (equivalent to 3.5 mg Neomycin), Polymixin B Sulfate-5000 I.U., Bacitracin Zinc-400 I.U.


  • PURPOSE

    PURPOSE: FIRST AID ANTIBIOTIC


  • INDICATIONS & USAGE

     FIRST AID TO HELP PREVENT INFECTION IN MINOR CUTS, BURNS, SCRAPES


  • WARNINGS

    FOR EXTERNAL USE ONLY.  DO NOT USE IN THE EYES.  DO NOT USE IF YOU ARE ALLERGIC TO ANY OF THE INGREDIENTS DUE TO THE POSSIBILITY OF ANAPHYLACTIC SHOCK.

    STOP USE AND ASK A DOCTOR BEFORE USE IN CASES OF DEEP PUNCTURE WOUNDS, ANIMAL BITES, 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 RIGHT AWAY





  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN


  • DOSAGE & ADMINISTRATION

     CLEAN THE AFFECTED AREA.  APPLY A SMALL AMOUNT OF 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


  • PRINCIPAL DISPLAY PANEL

    MM1USC Triple tube carton


  • INGREDIENTS AND APPEARANCE
    ULTRA SEAL TRIPLE ANTIBIOTIC  
    neomycin, polymixin, bacitracin ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:42213-360
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B SULFATE 5000 [iU]  in 1 g
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC 400 [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:42213-360-80 144 in 1 BOX
    1 NDC:42213-360-09 0.9 g in 1 PACKET
    2 NDC:42213-360-28 1 in 1 CARTON
    2 28 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 04/12/2011
    Labeler - Ultra Seal Corporation (085752004)
    Registrant - ULTRAtab Laboratories, Inc. (151051757)
    Establishment
    Name Address ID/FEI Business Operations
    ULTRAtab Laboratories, Inc. 151051757 manufacture