NEOSPORIN PLUS PAIN RELIEF- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride 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.

----------

NEOSPORIN ® + PAIN RELIEF OINTMENT

Drug Facts

Active ingredients (in each gram)Purpose
Bacitracin Zinc (500 units) First aid antibiotic
Neomycin Sulfate (3.5 mg) First aid antibiotic
Polymyxin B Sulfate (10,000 units) First aid antibiotic
Pramoxine HCl (10 mg)External analgesic

Uses

first aid to help prevent infection and for the temporary relief of pain 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
  • symptoms persist for more than 1 week, or clear up and occur again within a few days
  • rash or other allergic reaction develops

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Centre right away.

Directions

Other information

Inactive ingredient

Petrolatum

Questions?

call 800-223-0182 or 215-273-8755 (collect)

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 28.3 g Tube Carton

#1
DOCTOR
RECOMMENDED
BRAND

NEOSPORIN ®
+
PAIN RELIEF

Maximum Strength
Pain Relief

24-Hour Infection
Protection

Soothes Cuts, Scrapes
and Burns

NO STING

OINTMENT

FIRST AID ANTIBIOTIC/PAIN RELIEVING OINTMENT

Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate-
Pramoxine HCl

NET WT 1 oz (28.3 g)

Principal Display Panel - 28.3 g Tube Carton
NEOSPORIN PLUS PAIN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0057
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  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 B10000 [USP'U]  in 1 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0057-21 in 1 CARTON12/01/2009
114.2 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:69968-0057-11 in 1 CARTON12/01/2009
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 finalpart333B12/01/2009
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ee351b0e-75be-75a8-e053-2995a90a53ba
Set id: 32302dcd-f3f1-408b-ae5f-e7d8b666f68f
Version: 7
Effective Time: 20230111
 
Johnson & Johnson Consumer Inc.