NEOSPORIN PLUS BURN 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.

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NEOSPORIN ® + BURN RELIEF

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 ingredients

Petrolatum

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton

#1 DOCTOR
RECOMMENDED
BRAND
NEOSPORIN ®
+
BURN RELIEF
Maximum Strength
Pain Relief to
Soothe Minor Burns

24-Hour Infection
Protection

Triple Antibiotic
Formula

NO STING

OINTMENT
FIRST AID ANTIBIOTIC/ PAIN RELIEVING OINTMENT
Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate-
Pramoxine HCl
NET WT. 0.5 OZ (14.2 g)

PRINCIPAL DISPLAY PANEL - 14.2 g Tube Carton
NEOSPORIN PLUS BURN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0518
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [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 B10000 [iU]  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:69968-0518-11 in 1 CARTON02/01/2019
114.2 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B02/01/2019
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: eeac9760-b681-9586-e053-2a95a90a6a2e
Set id: 3caa7fd1-bd66-427e-a6c0-1b137b205089
Version: 4
Effective Time: 20230111
 
Johnson & Johnson Consumer Inc.