Home > Drugs A-Z > bacitracin zinc, neomycin sulfate and polymyxin b sulfate

bacitracin zinc, neomycin sulfate and polymyxin b sulfate (Dynarex Corporation)

Available Formats

Dosage Form Package Information Links
OINTMENT 72 TUBE in 1 CASE (67777-217-04) > 113.4 g in 1 TUBE Label Information
OINTMENT 1728 PACKET in 1 CASE (67777-217-08) > .9 g in 1 PACKET Label Information
OINTMENT 72 TUBE in 1 CASE (67777-217-03) > 56.7 g in 1 TUBE Label Information
OINTMENT 12 JAR in 1 CASE (67777-217-09) > 425.3 g in 1 JAR Label Information
OINTMENT 72 TUBE in 1 CASE (67777-217-01) > 28.35 g in 1 TUBE Label Information
OINTMENT 12 BOX in 1 CASE (67777-217-07) > 144 PACKET in 1 BOX > .9 g in 1 PACKET Label Information
OINTMENT 12 BOX in 1 CASE (67777-217-05) > 144 PACKET in 1 BOX > .5 g in 1 PACKET Label Information
OINTMENT 1728 PACKET in 1 CASE (67777-217-06) > .5 g in 1 PACKET Label Information
OINTMENT 72 TUBE in 1 CASE (67777-217-02) > 14.17 g in 1 TUBE Label Information

Complete bacitracin zinc, neomycin sulfate and polymyxin b sulfate Information

  • ACTIVE INGREDIENT

    Active ingredient (in ea. gram)                                                Purpose           
    Bacitracin Zinc 400 Units                                                          First Aid Antibiotic

    Neomyxin Sulfate 5mg (Equivalent to 3.5 mg Neomyxin)              First Aid Antibiotic

    Polymyxin B Sulfate 5000 Units                                                 First Aid Antibiotic


  • Ask a doctor before use:

    First aid to help prevent infection in:

    • Minor cuts
    • scrapes
    • burns

  • Purpose

    First aid to help prevent infection in:

    • Minor cuts
    • scrapes
    • burns

  • Other information

    • store at controlled room temperature 15°-30° C (59°-86° F)
    • avoid excessive heat and humidity

  • Inactive ingredients:

    Hard Paraffin, Liquid Paraffin, White Soft Paraffin


  • Keep Out Of Reach Of Children

    KEEP OUT OF REACH OF CHILDREN


  • Warnings

    For external use only


  • Dosage and Administration

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

  • 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

  • Stop use and ask a doctor if

    • Stop use and ask a doctor if condition persists or gets worse, or if a rash or other allergic reaction occurs

  • Principal Display panel

    Dynarex Triple Antibiotic


    triple-antibiotic-ointment-1184-01.jpg

    Triple Antibiotic


  • INGREDIENTS AND APPEARANCE
    BACITRACIN ZINC, NEOMYCIN SULFATE AND POLYMYXIN B SULFATE 
    bacitracin zinc, neomycin sulfate and polymyxin b sulfate ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-217
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [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:67777-217-01 28.35 g in 1 TUBE; Type 0: Not a Combination Product 04/18/2016
    2 NDC:67777-217-02 14.17 g in 1 TUBE; Type 0: Not a Combination Product 04/18/2016
    3 NDC:67777-217-05 0.5 g in 1 PACKET; Type 0: Not a Combination Product 04/18/2016
    4 NDC:67777-217-06 0.5 g in 1 PACKET; Type 0: Not a Combination Product 04/18/2016
    5 NDC:67777-217-07 0.9 g in 1 PACKET; Type 0: Not a Combination Product 04/18/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 12/01/2009
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)
    Establishment
    Name Address ID/FEI Business Operations
    Galentic Pharma (India) Pvt. Ltd. 650970176 manufacture(67777-217)