NORTH TRIPLE ANTIBIOTIC- bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment 
Honeywell Safety Products USA, Inc

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.

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0498-0750 & 0498-0740: Triple Antibiotic Ointment

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

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

Other information

Inactive ingredient

petrolatum

Questions?

1-800-430-5490

Principal Display Panel

triple

Honeywell Triple Antibiotic

Honeywell Triple

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)

Revised: 1/2024
Document Id: 0f8b8306-29aa-9088-e063-6294a90a527d
Set id: bb7b2064-6ed1-4e0a-9688-e2805a58a598
Version: 15
Effective Time: 20240118
 
Honeywell Safety Products USA, Inc