BACITRACIN ZINC- first aid antibiotic ointment

Bacitracin Zinc by

Drug Labeling and Warnings

Bacitracin Zinc by is a Otc medication manufactured, distributed, or labeled by Aldermed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Bacitracin Zinc (500 units in each gram)

Purpose

First Aid Antibiotic

Uses

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

Warnings

For external use only

Do not use

• In the eyes or apply over large areas of the body
• If you are allergic to any of the ingredients
• Longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

the condition persists or gets worse

if a 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

• Do not use if seal on the tube is damaged or is not visible
• To open,unscrew cap, pull tab to remove foil seal
• Store at room temperature
• Avoid excessive heat and humidity
• Preserve in well-closed container
• See crimp of tube or carton for Lot Number and Expiry Date

Inactive Ingredients

Mineral Oil, Paraffin, White Petrolatum

Questions?

Call 1-833-605-84-74 9am-5 pm EST M-F

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BACITRACIN ZINC 
first aid antibiotic ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-001
Route of Administration	TOPICAL

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

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87236-001-14	1 in 1 CARTON	11/01/2025
1		14.2 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 87236-001-01	1 in 1 CARTON	11/01/2025
2		28.4 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 87236-001-15	425 g in 1 JAR; Type 0: Not a Combination Product	11/01/2025
4	NDC: 87236-001-44	144 in 1 CARTON	11/01/2025
4		0.9 g in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 87236-001-09	0.9 g in 1 PACKET; Type 0: Not a Combination Product	11/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	11/01/2025

Labeler - Aldermed Inc. (144887712)