MEDICHOICE TRIPLE ANTIBIOTIC- bacitracin ointment

MediChoice Triple Antibiotic by

Drug Labeling and Warnings

MediChoice Triple Antibiotic by is a Otc medication manufactured, distributed, or labeled by Owens & Minor Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Bacitracin 400 units

Neomycin Sulfate 5 mg (Equivalent to 3.5 mg. Neomycin)

Polymyxin B Sulfate 5000 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 or over large areas of the body.  In case of deep puncture wounds, animal bites, or serious burns, consult a doctor.  Do not use if you are allergic to any of the ingredients. Do not use longer than 1 week unless directed by a doctor

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 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:

Tamper Evident. Do not use if packet is torn, cut or opened.
Avoid excessive heat and humidity
Store at a controlled room temperature 15˚ to 30˚C (59˚ to 86˚F)

Inactive Ingredients:

white petrolatum.

Product Labels

INGREDIENTS AND APPEARANCE

MEDICHOICE TRIPLE ANTIBIOTIC 
bacitracin ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 39892-0830
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [iU]  in 1 g
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN	5 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
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 39892-0830-1	144 in 1 CARTON	03/27/2015
1		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	03/27/2015

Labeler - Owens & Minor Inc. (847412269)

Registrant - Owens & Minor Inc. (847412269)

Establishment
Name	Address	ID/FEI	Business Operations
Ultra Seal Corporation		085752004	manufacture(39892-0830)