Label: NORTH TRIPLE ANTIBIOTIC- bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
TRIPLE ANTIBIOTIC- bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment

  • NDC Code(s): 0498-0740-01, 0498-0740-02, 0498-0740-03, 0498-0740-32, view more
    0498-0740-33, 0498-0740-34, 0498-0740-35, 0498-0740-36, 0498-0740-37, 0498-0740-38, 0498-0740-39, 0498-0750-02, 0498-0750-03, 0498-0750-34, 0498-0750-35, 0498-0750-36, 0498-0750-38, 0498-0750-39
  • Packager: Honeywell Safety Products USA, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 18, 2024

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  • Active Ingredients (each gram contains)

    Bacitracin zinc 400 units



    Neomycin sulfate (5 mg equivalent to 3.5 mg Neomycin base)



    Polymyxin B sulfate 5000 units

  • Purpose

    First aid antibiotic

    First aid antibiotic

    First aid antibiotic

  • Uses

    • first aid to help prevent infection in

    • minor cuts
    • scrapes
    • burns

  • Warnings

    For external use only

    Allergy alert do not use if you are allergic to any of the ingredients

    Do not use

    • in the eyes
    • over large areas of the body

    Ask a doctor before use if you have

    • a deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • the condition persists or gets worse
    • a rash or other allergic reaction develops
    • you need to use longer than 1 week

    Keep out of the 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 the 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 15 o to 25 oC (59 o to 77 o F)
    • tamper evident sealed packets
    • do not use if packet is torn or opened
  • Inactive ingredient

    petrolatum

  • Questions?

    1-800-430-5490

  • Principal Display Panel

    triple

  • Honeywell Triple Antibiotic

    Honeywell Triple

  • INGREDIENTS AND APPEARANCE
    NORTH TRIPLE ANTIBIOTIC 
    bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0740
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [iU]  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [iU]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0740-350.9 g in 1 PACKET; Type 0: Not a Combination Product03/07/201309/19/2018
    2NDC:0498-0740-02144 in 1 BOX, UNIT-DOSE03/07/201309/19/2018
    20.9 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:0498-0740-0325 in 1 BOX, UNIT-DOSE03/07/201312/19/2017
    30.9 g in 1 PACKET; Type 0: Not a Combination Product
    4NDC:0498-0740-011728 in 1 CARTON03/07/201312/19/2017
    40.9 g in 1 PACKET; Type 0: Not a Combination Product
    5NDC:0498-0740-3220 in 1 BOX, UNIT-DOSE03/07/201312/19/2017
    50.9 g in 1 PACKET; Type 0: Not a Combination Product
    6NDC:0498-0740-33100 in 1 BOX, UNIT-DOSE03/07/201312/19/2017
    60.9 g in 1 PACKET; Type 0: Not a Combination Product
    7NDC:0498-0740-3410 in 1 BOX, UNIT-DOSE03/07/201309/19/2018
    70.9 g in 1 PACKET; Type 0: Not a Combination Product
    8NDC:0498-0740-360.5 g in 1 PACKET; Type 0: Not a Combination Product03/07/201309/19/2018
    9NDC:0498-0740-37144 in 1 BOX, UNIT-DOSE03/07/201312/19/2017
    90.5 g in 1 PACKET; Type 0: Not a Combination Product
    10NDC:0498-0740-3872 in 1 BOX, UNIT-DOSE03/07/201309/19/2018
    100.5 g in 1 PACKET; Type 0: Not a Combination Product
    11NDC:0498-0740-39144 in 1 BOX03/07/201309/19/2018
    11NDC:0498-0740-360.5 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/07/201309/19/2018
    TRIPLE ANTIBIOTIC 
    bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0750
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [iU]  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [iU]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0750-350.9 g in 1 PACKET; Type 0: Not a Combination Product09/19/2018
    2NDC:0498-0750-02144 in 1 BOX09/19/2018
    20.9 g in 1 PACKET; Type 0: Not a Combination Product
    3NDC:0498-0750-0325 in 1 BOX09/19/2018
    30.9 g in 1 PACKET; Type 0: Not a Combination Product
    4NDC:0498-0750-3410 in 1 BOX09/19/2018
    40.9 g in 1 PACKET; Type 0: Not a Combination Product
    5NDC:0498-0750-360.5 g in 1 PACKET; Type 0: Not a Combination Product09/19/2018
    6NDC:0498-0750-3872 in 1 BOX09/19/2018
    60.5 g in 1 PACKET; Type 0: Not a Combination Product
    7NDC:0498-0750-39144 in 1 BOX09/19/2018
    7NDC:0498-0750-360.5 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/19/2018
    Labeler - Honeywell Safety Products USA, Inc (118768815)
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