TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment 
Taro Pharmaceuticals U.S.A., Inc.

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Triple Antibiotic

Drug Facts

Active ingredients (in each gram)Purpose
Bacitracin zinc USP 400 unitsFirst aid antibiotic
Neomycin sulfate USP 3.5 mgFirst aid antibiotic
Polymyxin B sulfate USP 5,000 unitsFirst aid antibiotic

Uses

first aid to help prevent infection in minor:

Warnings

For external use only.

Do not use

  • if you are allergic to any of the ingredients
  • in the eyes
  • over large areas of the body

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

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

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive ingredients

cocoa butter, cottonseed oil, olive oil, sodium pyruvate, vitamin E, white petrolatum

Questions?

Call 1-866-923-4914

Distributed by:
Taro Pharmaceuticals U.S.A., Inc.
Hawthorne, NY 10532

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

Original Strength

Triple Antibiotic
Ointment

Bacitracin Zinc USP • Neomycin Sulfate USP • Polymyxin B Sulfate USP

First Aid Antibiotic Ointment

NET WT 1 oz (28.4 g)

Principal Display Panel - 28.4 g Tube Carton
TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51672-2120
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
COCOA BUTTER (UNII: 512OYT1CRR)  
COTTONSEED OIL (UNII: H3E878020N)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
SODIUM PYRUVATE (UNII: POD38AIF08)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51672-2120-11 in 1 CARTON12/15/2015
114.2 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:51672-2120-21 in 1 CARTON12/15/2015
228.4 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:51672-2120-31 in 1 CARTON12/15/2015
360 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:51672-2120-66 in 1 CARTON09/20/2021
40.9 g in 1 APPLICATOR; Type 0: Not a Combination Product
5NDC:51672-2120-815 in 1 CARTON09/20/2021
50.9 g in 1 APPLICATOR; Type 0: Not a Combination Product
6NDC:51672-2120-9144 in 1 CARTON09/20/2021
60.9 g in 1 APPLICATOR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00412/15/2015
Labeler - Taro Pharmaceuticals U.S.A., Inc. (145186370)
Establishment
NameAddressID/FEIBusiness Operations
Taro Pharmaceuticals Inc.206263295manufacture(51672-2120)

Revised: 4/2024
Document Id: 1701f87e-c8a3-042d-e063-6394a90a88c3
Set id: d77239e6-5e81-439a-b0cd-f8be59169442
Version: 4
Effective Time: 20240426
 
Taro Pharmaceuticals U.S.A., Inc.