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 unitsFirst aid antibiotic
Neomycin Sulfate 3.5 mgFirst aid antibiotic
Polymyxin B sulfate 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

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 (collect)

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 0.9 g Packet Carton

#1
DOCTOR
RECOMMENDED
BRAND

ORIGINAL OINTMENT

NEOSPORIN ®

Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate

FIRST AID ANTIBIOTIC OINTMENT

Every Cut.
Every Time. ®

144 PACKETS 1/32 oz (0.9 g) each

NET WT 4.5 oz (130 g)

Principal Display Panel - 0.9 g Packet Carton
NEOSPORIN ORIGINAL 
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0634
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
SODIUM PYRUVATE (UNII: POD38AIF08)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
PETROLATUM (UNII: 4T6H12BN9U)  
LEVANT COTTONSEED OIL (UNII: N5CFT140R8)  
OLIVE OIL (UNII: 6UYK2W1W1E)  
COCOA BUTTER (UNII: 512OYT1CRR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0634-10.9 g in 1 POUCH; Type 0: Not a Combination Product01/04/2021
2NDC:69968-0634-9144 in 1 CARTON01/04/2021
20.9 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B01/04/2021
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: eed93bc3-352e-9e14-e053-2a95a90ae36c
Set id: f07d3bca-4312-46ed-b0c4-f886c01bd095
Version: 2
Effective Time: 20230109
 
Johnson & Johnson Consumer Inc.