NEOSPORIN ORIGINAL- bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment 
Johnson & Johnson Consumer Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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NEOSPORIN ORIGINAL OINTMENT

Drug Facts

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

Use

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 1-800-223-0182

PRINCIPAL DISPLAY PANEL - 14.2 g Carton

ORIGINAL OINTMENT

NEOSPORIN®

Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate
FIRST AID ANTIBIOTIC OINTMENT

NET WT 0.5 oz (14.2 g)

PRINCIPAL DISPLAY PANEL - 14.2 g Carton
NEOSPORIN ORIGINAL 
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-4002
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:58232-4002-10.9 g in 1 POUCH; Type 0: Not a Combination Product08/03/201106/14/2018
2NDC:58232-4002-21 in 1 CARTON08/03/201106/14/2018
214.2 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:58232-4002-61 in 1 CARTON08/03/201107/18/2018
328.3 g in 1 TUBE; Type 0: Not a Combination Product
4NDC:58232-4002-9144 in 1 CARTON08/03/2011
40.9 g in 1 POUCH; Type 0: Not a Combination Product
5NDC:58232-4002-80.9 g in 1 POUCH; Type 0: Not a Combination Product08/03/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/03/2011
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 9/2021
Document Id: cb1603c2-e8eb-b459-e053-2995a90aec60
Set id: b6697cce-f370-4f7b-8390-9223a811a005
Version: 10
Effective Time: 20210903
 
Johnson & Johnson Consumer Inc.