TRIPLE ANTIBIOTIC CVS- bacitracin, neomycin, polymyxin ointment

Triple Antibiotic by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Bacitracin 400 units, Neomycin 3.5 mg, Polymyxin B 5000 units

INDICATIONS & USAGE

Uses

First aid to help prevent infection and for temporary relief of pain or discomfort in minor: cuts, scrapes, and burns.

WARNINGS

Warnings

For external use only. Do not use in the eyes, over large areas of the body.  When using this product keep out of eyes.  Rinse eyes with water to remove.  Do not puncture or incinerate.  Contents under pressure. Ask a doctor before use if you have condition or symptoms get worse or last more than one week, symptoms clear up and occur again within a few days.

DOSAGE & ADMINISTRATION

Directions

Adults and children 2 years of age and older:  clean the affected area, shake well before each use, spray a small amount of the product on the area 1 to 3 times daily.  May be covered with a sterile bandage.  Children under 2 years of age: consult a doctor.

INACTIVE INGREDIENT

Inactive ingredients

Glycerin, Hydrogenated Styrene/Butadiene Copolymer, Mineral Oil, Pentylene Glycol

PURPOSE

Purpose

First aid antibiotic.

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TRIPLE ANTIBIOTIC  CVS
bacitracin, neomycin, polymyxin ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-047
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
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	500 U  in 1 g
BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	400 U  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Glycerin (UNII: PDC6A3C0OX)
Mineral Oil (UNII: T5L8T28FGP)
Pentylene Glycol (UNII: 50C1307PZG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-047-02	56 g in 1 CAN; Type 0: Not a Combination Product	02/14/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333B	02/14/2014

Labeler - CVS (062312574)