POLYSPORIN- polymyxin b sulfate and bacitracin zinc powder

Polysporin by

Drug Labeling and Warnings

Polysporin 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 500 units: First aid antibiotic
• Polymyxin B 10,000 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 light dusting of the powder 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)
• do not refrigerate

Inactive ingredient

lactose base

Questions?

call 1-800-223-0182

PRINCIPAL DISPLAY PANEL - 10g Bottle Label

#1
DERMATOLOGIST
RECOMMENDED

Polysporin®

BACITRACIN ZINC POLYMYXIN B SULFATE
First Aid Antibiotic Powder

Helps prevent infection in minor cuts, scrapes, and burns

NET WT 0.35 oz (10g)

INGREDIENTS AND APPEARANCE

POLYSPORIN 
polymyxin b sulfate and bacitracin zinc powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58232-4033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Polymyxin B Sulfate (UNII: 19371312D4) (Polymyxin B - UNII:J2VZ07J96K)	Polymyxin B	10000 [USP'U]  in 1 g
Bacitracin Zinc (UNII: 89Y4M234ES) (Bacitracin - UNII:58H6RWO52I)	Bacitracin	500 [USP'U]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58232-4033-1	1 in 1 CARTON	06/14/2010	12/01/2023
1		10 g in 1 BOTTLE; 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	06/14/2010	12/01/2023

Labeler - Johnson & Johnson Consumer Inc. (002347102)