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

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Triple Antibiotic

Medline Industries, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient (in each gram)

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg (Equivalent to 3.5 mg. Neomycin)

Polymyxin B Sulfate 5000 units

Purpose

Antibacterial

Triple Antibiotic Uses

First aid to help prevent infection in

  • minor cuts
  • scrapes
  • burns

Warnings

For external use

Do not use

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

Stop use and ask a doctor if

  • before use in case of deep puncture wounds, animal bites or serious burns
  • if the condition persists or gets worse
  • if 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.
  • 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

  • Protect from freezing. Avoid excessive heat.
  • Do not use if packet is torn, cut or opened.

Inactive ingredients

Petrolatum

Package/Label Principal Display Panel

Triple Antibiotic
Triple Antibiotic Ointment Box

CURAD

TRIPLE ANTIBIOTIC OINTMENT

first aid antibiotic

NET WT. 1 oz (28.4 g)

Triple Antibiotic

bacitracin zinc, neomycin sulfate, polymyxin B sulfate OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53329-087
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

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

Inactive Ingredients

Ingredient Name Strength
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 28.4 in 1 TUBE
2 NDC:53329-087-87 0.9 in 1 PACKET
3 NDC:53329-087-96 144 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part333 2010-04-01


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Be sure to consult your doctor before taking any medication!
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