TRIPLE ANTIBIOTIC ointment

Triple Antibiotic by

Drug Labeling and Warnings

Triple Antibiotic by is a Otc medication manufactured, distributed, or labeled by B8 Sales, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Triple Antibiotic Ointment™

First Aid to Help Prevent Infection In Minor Cuts, Scrapes, and Burns

25 Packets

Each Packet Net.Wt.0.9gm

Drug Facts

Active ingredients (in each gram)

Bacitradn Zinc (400 units Bacitracin)

Neomycin Sulfate 5 mg

(equivalent to 3.5 mg Neomycin base)

Polymyxin-B Sulfate 5000 units

Purpose

First aid antibiotic

Uses

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

Warnings

For external use only

Do not use

• in the eyes
• internally
• over large areas of the body
• if you are allergic to any of the ingredients
• longer than 1 week unless directed by a doctor

Stop use and ask a doctor If

• the condition persists or gets worse
• a rash or other allergic reaction develops

Keep out reach of children. If swallowed, get

medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years and over:

• 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 dally
• may be covered with a sterile bandage

Children under 2 years:

• consult a doctor

Other information

• store at room temperature (do not freeze)
• do not use any opened or torn packets

Inactive ingredients

petrolatum

Triple Antibiotic Ointment™

Manufactured for:

B8 SALES

Cincinnati,0hio 4521S

888-826-6208

www.b8sales.com

PIO Put it on®

Principal Display Panel

Triple Antibiotic Ointment – Carton Label

PIO Put it on®

Triple Antibiotic Ointment™

First Aid to Help Prevent Infection In Minor Cuts, Scrapes, and Burns

25 Packets

Each Packet Net.Wt.0.9gm

INGREDIENTS AND APPEARANCE

TRIPLE ANTIBIOTIC 
triple antibiotic ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50607-5600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Bacitracin Zinc (UNII: 89Y4M234ES) (Bacitracin Zinc - UNII:89Y4M234ES)	Bacitracin Zinc	400   in 1 g
Neomycin Sulfate (UNII: 057Y626693) (Neomycin - UNII:I16QD7X297)	Neomycin Sulfate	5 mg  in 1 g
Polymyxin B Sulfate (UNII: 19371312D4) (Polymyxin B - UNII:J2VZ07J96K)	Polymyxin B Sulfate	5000   in 1 g

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

Product Characteristics
Color	white (white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50607-5600-1	25 in 1 BOX
1		.9 g in 1 POUCH
2	NDC: 50607-5600-2	144 in 1 BOX
2		.9 g in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333	05/01/2010

Labeler - B8 Sales, Inc. (833208635)