UEC MEDICAL FIRST AID ANTIBIOTIC- bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment

UEC Medical First Aid Antibiotic by

Drug Labeling and Warnings

UEC Medical First Aid Antibiotic by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients Purpose

Bacitracin zinc 400 units..............................................................First aid antibiotic

Neomycin sulfate 5 mg (equivalent to 3.5 mg Neomycin)............First aid antibiotic

Polymyxin B sulfate 5,000 units...................................................First aid antibiotic

PURPOSE

Uses

first aid to help prevent infection in minor:

• cuts
• scrapes
• burns

WARNINGS

Warnings

For external use only.

DO NOT USE

Do not use

• if you are allergic to any of the ingredients
• in the eyes
• over large areas of the body

ASK DOCTOR

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

STOP USE

Stop use and ask a doctor if

• you need to use longer than 1 week
• condition persists or gets worse
• rash or other allergic reaction develops

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

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

STORAGE AND HANDLING

Other information

• store at 15° to 25°C (59° to 77°F)

INACTIVE INGREDIENT

Inactive ingredients

white soft paraffin

DOSAGE & ADMINISTRATION

Distributed by:

UEC Medical

17211 Valley View Ave.

Cerritos, CA 90703

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UEC MEDICAL FIRST AID ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, and polymyxin b sulfate ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-391
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297)	NEOMYCIN SULFATE	3.5 mg  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K)	POLYMYXIN B	5000 [iU]  in 1 g
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 [iU]  in 1 g

Inactive Ingredients
Ingredient Name	Strength
PARAFFIN (UNII: I9O0E3H2ZE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-391-20	20 in 1 BOX	04/04/2016
1		0.5 g in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 65923-391-44	144 in 1 BOX	04/04/2016
2		0.5 g in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 65923-391-21	20 in 1 BOX	04/04/2016
3		0.9 g in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 65923-391-45	144 in 1 BOX	04/04/2016
4		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	04/04/2016

Labeler - United Exchange Corp. (840130579)