NEOSPORIN ORIGINAL- bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment

Neosporin Original by

Drug Labeling and Warnings

Neosporin Original by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients (in each gram)	Purpose
Bacitracin 400 units	First aid antibiotic
Neomycin 3.5 mg	First aid antibiotic
Polymyxin B 5,000 units	First 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 - 14.2 g Carton

ORIGINAL OINTMENT

NEOSPORIN®

Bacitracin Zinc-Neomycin Sulfate-Polymyxin B Sulfate
FIRST AID ANTIBIOTIC OINTMENT

NET WT 0.5 oz (14.2 g)

INGREDIENTS AND APPEARANCE

NEOSPORIN ORIGINAL 
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58232-4002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Bacitracin Zinc (UNII: 89Y4M234ES) (Bacitracin - UNII:58H6RWO52I)	Bacitracin	400 [iU]  in 1 g
Neomycin Sulfate (UNII: 057Y626693) (Neomycin - UNII:I16QD7X297)	Neomycin	3.5 mg  in 1 g
Polymyxin B Sulfate (UNII: 19371312D4) (Polymyxin B - UNII:J2VZ07J96K)	Polymyxin B	5000 [iU]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Cocoa Butter (UNII: 512OYT1CRR)
Cottonseed Oil (UNII: H3E878020N)
Olive Oil (UNII: 6UYK2W1W1E)
Sodium Pyruvate (UNII: POD38AIF08)
.Alpha.-Tocopherol (UNII: H4N855PNZ1)
Petrolatum (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58232-4002-1	0.9 g in 1 POUCH; Type 0: Not a Combination Product	08/03/2011	06/14/2018
2	NDC: 58232-4002-2	1 in 1 CARTON	08/03/2011	06/14/2018
2		14.2 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 58232-4002-6	1 in 1 CARTON	08/03/2011
3		28.3 g in 1 TUBE; Type 0: Not a Combination Product
4	NDC: 58232-4002-9	144 in 1 CARTON	08/03/2011
4		0.9 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part333B	08/03/2011

Labeler - Johnson & Johnson Consumer Inc. (002347102)