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

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Genuine Triple Antibiotic

Genuine First Aid LLC

Genuine Triple Antibiotic


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Active Ingredient: .........Bacitracin Zinc 400 units

Neomycin Sulfate 5mg ( equivalent to 3.5 mg Neomycin base)

Polymyxin B Sulfate 5000 units

Purpose

Triple Antibiotic

Uses

Uses:  To help prevent infection in:
minor cuts;  scrapes;  burns

Warnings


For external use only.

Do not use:  in eyes;  over large areas of the body;

If allergic to any of the ingredients;  for more than one week unless directed by a physician.

Stop use and consult a doctor:

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

Keep out of reach of children.

If ingested, contact a Poison

Control Center right away.

Directions

Directions: clean affected area;  apply 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.

Inactive Ingredient




Genuine Triple Antibiotic

First Aid Ointment

To Help Prevent Infection

Each Gram Contains:

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg

(equivalent to 3.5 mg

Neomycin base)

 Polymyxin B Sulfate 5000 units

Net Wt. 0.5g ; (1/64 oz)

Manufactured in CHINA for

GENUINE FIRST AID.



Triple Antibiotic Ointment 10pcs

Net wt. 0.9g (1/32oz)



100
Triple Antibiotic

Genuine Triple Antibiotic

Genuine Triple Antibiotic

BACITRACIN ZINC,NEOMYCIN SULFATE,POLYMYXIN B SULFATE OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52124-0003
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BACITRACIN ZINC BACITRACIN 400 [iU]
Neomycin Sulfate NEOMYCIN 5 mg
Polymyxin B Sulfate POLYMYXIN B 5000 [iU]

Inactive Ingredients

Ingredient Name Strength
petrolatum
Mineral Oil
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52124-0003-1 0.5 in 1 TUBE
2 0.5 in 1 PACKET
3 0.5 in 1 PACKET
4 NDC:52124-0003-3 100 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2010-02-16


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