Triple Antibiotic description, usages, side effects, indications, overdosage, supplying and lots more!

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Triple Antibiotic

Taro Pharmaceuticals U.S.A., Inc.

Triple Antibiotic


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients (each gram contains) Purpose
Bacitracin zinc 400 units First aid antibiotic
Neomycin sulfate 3.5 mg First aid antibiotic
Polymyxin B sulfate 5,000 units First aid antibiotic

Triple Antibiotic Uses

first aid to help prevent infection in

  • minor cuts
  • scrapes
  • burns

Warnings

For external use only

Do not use

  • in the eyes
  • over large areas of the body
  • if you are allergic to any of the ingredients
  • longer than 1 week

Ask a doctor before use

  • on deep or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

  • condition persists 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 right away.

Directions

  • clean the affected area and dry thoroughly
  • 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

Triple Antibiotic Other information

  • To open: unscrew cap, pull tab to remove foil seal
  • store at room temperature
  • see carton or tube crimp for lot number and expiration date

Inactive ingredient

white petrolatum

Questions?

Call 1-866-923-4914

Distributed by:
Taro Pharmaceuticals
U.S.A., Inc.

Hawthorne, NY 10532

PRINCIPAL DISPLAY PANEL - 28.4 g Tube Carton

Triple Antibiotic
Ointment

First Aid Antibiotic Ointment

Original Strength

  • Bacitracin Zinc
  • Neomycin Sulfate
  • Polymyxin B Sulfate

NET WT 1 oz (28.4 g)

Triple Antibiotic

Triple Antibiotic

Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51672-2016
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BACITRACIN ZINC BACITRACIN 400 [iU]
Neomycin Sulfate NEOMYCIN 3.5 mg
Polymyxin B Sulfate POLYMYXIN B 5000 [iU]

Inactive Ingredients

Ingredient Name Strength
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 14.2 in 1 TUBE
2 28.4 in 1 TUBE
3 NDC:51672-2016-2 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 1995-12-14


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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