FIRST AID ANTIBIOTIC- bacitracin zinc ointment

First Aid Antibiotic by

Drug Labeling and Warnings

First Aid Antibiotic by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP, Ultra Seal Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each gram)

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

• in the eyes
• if you are allergic to any of the ingredients, due to the possibility of anaphylactic shock
• over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use

on 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 occurs

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

• Store at controlled room temperature 68º-77ºF (20º-25ºC)
• Use only if packaging is intact.

Inactive ingredients

mineral oil, petrolatum

Package Labels

INGREDIENTS AND APPEARANCE

FIRST AID ANTIBIOTIC 
bacitracin zinc ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-089
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)
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-089-01	1 in 1 BOX	03/01/2010
1		28.4 g in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 53329-089-86	144 in 1 CARTON	03/01/2010
2	NDC: 53329-089-87	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 final	part333B	03/01/2010

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
Ultra Seal Corporation		944090448	manufacture(53329-089)