Bacitracin Zinc description, usages, side effects, indications, overdosage, supplying and lots more!

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Bacitracin Zinc

A-S Medication Solutions LLC

Bacitracin Zinc Ointment USP


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient (in each gram):

Bacitracin Zinc (equal to 500 bacitracin units)

Purpose:

Antibiotic

Uses

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

Ask doctor before use in case of deep or puncture wounds, animal bites or serious burns

When using this product do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor 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

Other information:

  • do not use if seal is punctured or is not visible. To open, reverse cap to puncture seal
  • store at room temperature
  • see crimp of tube for Lot Number and Exp. Date

Inactive Ingredients

white petrolatum

Questions or comments? call toll free 1-800-645-9833

E. FOUGERA & CO.

A division of Fougera Pharmaceuticals Inc.

Melville, NY 11747

PRINCIPAL DISPLAY PANEL

NDC 54569-2409-0

Relabeled by:
A-S Medication Solutions
Libertyville, IL 60048


Bacitracin Zinc

Bacitracin Zinc

bacitracin zinc OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54569-2409(NDC:0168-0011)
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
BACITRACIN ZINC BACITRACIN 500 [USP'U]

Inactive Ingredients

Ingredient Name Strength
petrolatum

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 14.17 in 1 TUBE
2 NDC:54569-2409-0 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2010-01-08


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