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Neosporin Original by Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

Medically reviewed on August 31, 2017

Dosage form: kit
Ingredients: Bacitracin 400[iU] in 1g, Neomycin 3.5mg in 1g, Polymyxin B 5000[iU] in 1g
Labeler: Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.
NDC Code: 58232-0424

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 ORIGINAL OINTMENT

Drug Facts

Active ingredients (in each gram)Purpose
Bacitracin 400 unitsFirst aid antibiotic
Neomycin 3.5 mgFirst aid antibiotic
Polymyxin B 5,000 unitsFirst aid antibiotic

Use

first aid to help prevent infection in minor:

  • cuts
  • scrapes
  • burns

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
  • clean the affected area
  • apply a small amount of this product (an amount equal
    to the surface area of the tip of a finger) on the area
    1 to 3 times daily
  • may be covered with a sterile bandage

Other information
  • store at 20° to 25°C (68° to 77° F)

Inactive ingredients

cocoa butter, cottonseed oil, olive oil, sodium pyruvate, vitamin E, white petrolatum

Questions?

call 1-800-223-0182

Dist: Johnson & Johnson Consumer
Products Company Division of
Johnson & Johnson
Consumer Companies, Inc.
Skillman, NJ 08558 USA

PRINCIPAL DISPLAY PANEL - 70.8 g Kit

NDC# 58232-0424-1

Patented
TECHNOLOGY

2 Days Faster Results*Every Cut.
Every Time®
NEOSPORIN®
Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate
FIRST AID ANTIBIOTIC OINTMENT
NET WT 2.5 OZ (70.8 g) *Visibly healthier skin than generic
triple antibiotic ointments
CONTAINS:
2 Tubes - NEOSPORIN® Original First Aid Antibiotic Ointment
   1 oz (28.3 g) each NET WT 2 oz (56.6 g)
1 Tube - NEOSPORIN® Original First Aid Antibiotic Ointment 0.5 oz (14.2 g)
NEOSPORIN ORIGINAL 
bacitracin, neomycin, polymyxin b kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-0424
Packaging
#Item CodePackage Description
1NDC:58232-0424-11 KIT (KIT) in 1 BLISTER PACK
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 12 TUBE 56.6 g
Part 21 TUBE 14.2 g
Part 1 of 2
NEOSPORIN ORIGINAL 
bacitracin, neomycin, polymyxin b ointment
Product Information
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Bacitracin (Bacitracin) Bacitracin400 [iU]  in 1 g
Neomycin (Neomycin) Neomycin3.5 mg  in 1 g
Polymyxin B (Polymyxin B) Polymyxin B5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
Cocoa Butter 
Cottonseed Oil 
Olive Oil 
Sodium Pyruvate 
Alpha-Tocopherol 
Petrolatum 
Packaging
#Item CodePackage Description
12 TUBE (TUBE) in 1 CARTON
128.3 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/29/2011
Part 2 of 2
NEOSPORIN ORIGINAL 
bacitracin, neomycin, polymyxin b ointment
Product Information
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Bacitracin (Bacitracin) Bacitracin400 [iU]  in 1 g
Neomycin (Neomycin) Neomycin3.5 mg  in 1 g
Polymyxin B (Polymyxin B) Polymyxin B5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
Cocoa Butter 
Cottonseed Oil 
Olive Oil 
Sodium Pyruvate 
Alpha-Tocopherol 
Petrolatum 
Packaging
#Item CodePackage Description
11 TUBE (TUBE) in 1 CARTON
114.2 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/29/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/29/2011
Labeler - Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc. (830803164)

 
Johnson & Johnson Consumer Products Company, Division of Johnson & Johnson Consumer Companies, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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