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

Medically reviewed on August 8, 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: 58232-0423

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

PRINCIPAL DISPLAY PANEL - 56.7 G Blister Pack

NDC 58232-0423-1
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 OZ (56.7 G)*Visibly healthier skin than generic
triple antibiotic ointments

CONTAINS:
2 Tubes - NEOSPORIN® Original First Aid Antibiotic Ointment
               0.5 oz (14.2 g) each NET WT 1 oz (28.4 g)
1 Tube - NEOSPORIN® Original First Aid Antibiotic Ointment 1 oz (28.3 g)

NEOSPORIN ORIGINAL 
bacitracin, neomycin, polymyxin b kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58232-0423
Packaging
#Item CodePackage Description
1NDC:58232-0423-11 KIT (KIT) in 1 BLISTER PACK
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 12 TUBE 28.4 g
Part 21 TUBE 28.3 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
114.2 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/04/2011
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
128.3 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/04/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/04/2011
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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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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