PROCURE TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment

ProCure Triple Antibiotic by

Drug Labeling and Warnings

ProCure Triple Antibiotic by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg (equilvant to 3.5mg of Neomycin Base)

Polymyxin B Sulfate 5,000 units

Purpose

Purpose

First Aid Antibiotic

Uses

First aid to help prevent infection in minor:

• cuts
• scrapes
• burns

Warnings

Warnings

For External Use Only

Do not use

Do not use

• in the eyes
• if you are allergic to any of the ingredients
• over large areas of the body

Ask a doctor before use

Ask a doctor before use if you have:

• animal bites
• serious burns
• deep or puncture wounds

Keep out of reach of children

Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center immediately.

Directions

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

Inactive Ingredient

Inactive Ingredient: White Petrolatum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE TRIPLE ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-020
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	5000 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	5 mg  in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	400 [iU]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Product Characteristics
Color	white (Clear to white color)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-020-01	28.3 g in 1 TUBE; Type 0: Not a Combination Product	06/16/2025
2	NDC: 55681-020-14	144 in 1 CARTON	06/16/2025
2	NDC: 55681-020-09	0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	06/16/2025

Labeler - Twin Med LLC (009579330)