TRIPLE ANTIBIOTIC ointment

Triple Antibiotic by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active Ingredient (in each gram)

Bacitracin Zinc 400 units

Purpose

First Aid Antibiotic

Active Ingredient (in each gram)

Neomycin Sulfate 5 mg (equivalent to 3.5 mg Neomycin)

Purpose

First Aid Antibiotic

Active Ingredient (in each gram)

Polymyxin B Sulfate 5000 units

Purpose

First Aid Antibiotic

Use(s)

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

Warnings

For External Use Only

Do not use

In the eyes or apply 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, or serious burns

Stop use and ask a doctor if

The condition perists or gets worse

A rash or other allergic reaction develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) 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 between 15º-30ºC (59º-86ºF)

Tamper evident. Do not use if packet is torn, cut, or opened.

Inactive Ingredient

White Petrolatum

Questions?

1-888-900-2920 Monday - Friday 8AM-4PM PST.

Label

FL-2009

INGREDIENTS AND APPEARANCE

TRIPLE ANTIBIOTIC 
triple antibiotic ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58228-6209
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	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
WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58228-6209-1	1800 in 1 CASE	01/26/2024
1		25 in 1 BOX
1		0.5 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 Drug	M004	01/26/2024

Labeler - Front Line Safety (061263699)