CVS TRIPLE ANTIBIOTIC- bacitracin, neomycin, polymyxin b ointment

CVS Triple Antibiotic by

Drug Labeling and Warnings

CVS Triple Antibiotic by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients (in each gram)        

Bacitracin 400 units

Neomycin 3.5 mg

Polymyxin B 5,000 units

Uses

first aid to help prevent infection in minor:
cuts     scrapes    burns

Warnings

For external use only.

Do not use

if you are allergic to any of the ingredients

in the eyes

over large areas of the body

Ask a doctor before use if you have

deep or puncture wounds animal bites serious burns

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 side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

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 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

Inactive Ingredients

white petrolatum

Purpose

First Aid Antibiotic

Other information

store at controlled room temperature

prior to initial use, please prime pump by depressing multiple times

Questions or Comments?

1-800-635-3696

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS TRIPLE ANTIBIOTIC 
bacitracin, neomycin, polymyxin b ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-610
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
PETROLATUM (UNII: 4T6H12BN9U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-610-71	1 in 1 PACKAGE	11/01/2008
1		7.7 g in 1 BOTTLE; 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	11/01/2008

Labeler - CVS Pharmacy (062312574)