Bacitracin by AlderMed Inc. BACITRACIN ointment

Bacitracin by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

Active ingredient

Bacitracin USP (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 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, or if a rash or other allergic reaction develops.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Centre right away (1-800-222-1222)

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
• See crimp of tube or carton for Lot Number and Expiry Date

Inactive Ingredients

Mineral Oil, Paraffin, White Petrolatum

Questions?

Contact- 1-800-707-4621

Manufactured in India by:

Gopaldas Visram & Company Limited,

Plot No. A327, T.T.C. Indl. Area, M.I.D.C.

Mahape, Navi Mumbai - 400710.

Mfg. Lic. No.: KD/503

Principal Display Panel

INGREDIENTS AND APPEARANCE

BACITRACIN 
bacitracin ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	500 [iU]  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: 87236-000-09	1 in 1 CARTON	11/01/2025
1		0.9 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 87236-000-14	1 in 1 CARTON	11/01/2025
2		14.2 g in 1 TUBE; Type 0: Not a Combination Product
3	NDC: 87236-000-01	1 in 1 CARTON	11/01/2025
3		28.4 g in 1 TUBE; 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	11/01/2025

Labeler - AlderMed Inc. (144887712)