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 Zinc (400 units)First aid antibiotic
Neomycin Sulfate (3.5 mg)First aid antibiotic
Polymyxin B sulfate (5,000 units)First 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

Petrolatum, Gossypium Herbaceum (Cotton) Seed Oil, Olea Europaea (olive) Fruit Oil, Theobroma Cacao (Cocoa) Seed Butter, Sodium Pyruvate, Tocopheryl Acetate

Questions?

Call Toll Free 800-223-0182 or 215-273-8755

Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 28.3 g Tube Carton

#1
DOCTOR
RECOMMENDED
BRAND
NEOSPORIN ®
ORIGINAL

Triple Antibiotic Ointment
24-Hour Infection
Protection

Effective Germ
Kill Formula

NO STING

OINTMENT

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

NET WT 1 OZ (28.3 g)

PRINCIPAL DISPLAY PANEL - 28.3 g Tube Carton
NEOSPORIN ORIGINAL 
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0056
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
LEVANT COTTONSEED OIL (UNII: N5CFT140R8)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
COCOA BUTTER (UNII: 512OYT1CRR)  
SODIUM PYRUVATE (UNII: POD38AIF08)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0056-21 in 1 CARTON09/03/2016
114.2 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:69968-0056-11 in 1 CARTON09/03/2016
228.3 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B09/03/2016
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ee34b763-4be7-7080-e053-2995a90a202b
Set id: a3e6fe2e-1b74-4f22-9c7c-a00057439690
Version: 5
Effective Time: 20230111
 
Johnson & Johnson Consumer Inc.