PROCURE BACITRACIN ZINC- bacitracin zinc ointment

ProCure Bacitracin Zinc by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient

Bacitracin Zinc 500 units

Purpose

First Aid Antibiotic

Uses

First aid to help prevent infection in minor: cuts, scrapes, burns

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
• longer than 1 week unles directed by a doctor

Ask a doctor before use

Ask a doctor before use if you have:

• animal bites
• serious burns
• deep or puncture wounds

Stop use and ask a doctor

Stop use and ask a doctor if

• condition persists or gets worse
• rash or other allergic reaction develops

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

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 Ingredients

Inactive Ingredients: Mineral Oil, Paraffin, White Petrolatum

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE BACITRACIN ZINC 
bacitracin zinc ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN ZINC	500 [iU]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PARAFFIN (UNII: I9O0E3H2ZE)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)
MINERAL OIL (UNII: T5L8T28FGP)

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: 55681-016-01	28.3 g in 1 TUBE; Type 0: Not a Combination Product	06/05/2025
2	NDC: 55681-016-14	144 in 1 BOX	06/05/2025
2	NDC: 55681-016-09	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	06/05/2025

Labeler - Twin Med LLC (009579330)