NEOSPORIN PLUS PAIN RELIEF CLUBTRAY- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride 
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 Plus Pain Relief Clubtray

Neosporin Plus Pain 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 215-273-8755 (collect)

Distributed by:

JOHNSON & JOHNSON CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - Kit Package Label

#1 DOCTOR

RECOMMENDED

BRAND

OINTMENT

NEOSPORIN®

+

PAIN RELIEF

Maximum Strength Pain Relief

24-Hour Infection

Protection

Every Cut.

Every Time.®

Use with

BAND-AID®

Brand

Bandages

FIRST AID ANTIBIOTIC

PAIN RELIEVING

OINTMENT

Bacitracin Zinc-Neomycin

Sulfate-Polymyxin B

Sulfate-Pramoxine HCl

For Home

& On-the-Go!

NO STING

NEW WT 2.0 oz (56.7g)

CONTAINS:

1 Tube -

NEOSPORIN® + Pain Relief

Ointment 1 oz (28.3 g)

2 Tubes –

NEOSPORIN® + Pain Relief

Ointment 0.5 oz (14.2 g) each

Neosporin_01

NEOSPORIN PLUS PAIN RELIEF  CLUBTRAY
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0801
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0801-91 in 1 PACKAGE06/01/2022
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 TUBE 14.2 g
Part 21 TUBE 28.3 g
Part 1 of 2
NEOSPORIN PLUS PAIN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment
Product Information
Item Code (Source)NDC:69968-0057
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
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
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0057-21 in 1 CARTON
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 finalpart333B12/01/2009
Part 2 of 2
NEOSPORIN PLUS PAIN RELIEF 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride ointment
Product Information
Item Code (Source)NDC:69968-0057
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
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
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0057-11 in 1 CARTON
128.3 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
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B06/01/2022
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 2/2023
Document Id: f45439b8-0451-267b-e053-2995a90ae848
Set id: f4545718-8643-a340-e053-2995a90a0079
Version: 1
Effective Time: 20230210
 
Johnson & Johnson Consumer Inc.