NEOSPORIN PLUS PAIN RELIEF CLUBTRAY- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride 
Kenvue Brands LLC

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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 28.3 g
Part 21 TUBE 14.2 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:69968-0057-11 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 DrugM00412/01/2009
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:69968-0057-21 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 DrugM00412/01/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00406/01/2022
Labeler - Kenvue Brands LLC (118772437)

Revised: 11/2024
Document Id: 223f1589-0970-d83a-e063-6394a90a4207
Set id: f4545718-8643-a340-e053-2995a90a0079
Version: 2
Effective Time: 20241114
 
Kenvue Brands LLC