FIRST AID ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b sulfate gel

First Aid Antibiotic by

Drug Labeling and Warnings

First Aid Antibiotic by is a Otc medication manufactured, distributed, or labeled by Hubei Changjian Medical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients (in each gram)

Bacitracin zinc (bacitracin 400 units)

Neomycin sulfate (neomycin 3.5mg)

Polymyxin B sulfate (polymyxin B 5,000 units)

Purpose

First aid antibiotic

Use

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

Warnings

For external use only.

Do not use

• in the eyes
• 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
• serious burns

Stop use and ask a doctor if

• the condition persists or gets worse.
• a rash or other allergic reaction develops.

Keep out of reach of children.

lf 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 room temperature

Inactive ingredients

Mineral oil, petrolatum, purified water

Package Labeling: 82996-001-01

INGREDIENTS AND APPEARANCE

FIRST AID ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82996-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	35 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
PETROLATUM (UNII: 4T6H12BN9U)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82996-001-01	0.5 g in 1 POUCH; Type 0: Not a Combination Product	11/01/2022	04/01/2027

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	11/01/2022	04/01/2027

Labeler - Hubei Changjian Medical Products Co., Ltd. (699440035)