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

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Bacitracin Zinc

Dynarex Corporation
Dynarex Corporation

Bacitracin Zinc Ointment


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                         Purpose
Bacitracin Zinc 500 Units                Antibiotic

Warnings:

For external use only

DOSAGE & ADMINISTRATION:

  • clean the affected areas
  • apply a small amount of product (an amount equal to the surface area of the tip of the finger) on the area 1 to 3 times daily
  • may be covered with a sterile bandage

Stop use and ask a doctor if

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

Indications & Usage:

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

Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away

Purpose:

First aid to help prevent infection in:
Minor cuts
scrapes
burns

Ask a doctor before use:

  • in case of deep or puncture wounds
  • animal bites
  • serious burns

Bacitracin Zinc Other information

  • store at controlled room temperature 15°-30° C (59°-86° F)

Inactive ingredients

Hard Paraffin, Liquid Paraffin, White Soft Paraffin

Principal Display Panel

Dynarex Bacitracin Zinc Ointment:

bacitracin-zinc-galentic-1172-01.jpg


Bacitracin Zinc

Bacitracin Zinc

Bacitracin Zinc OINTMENT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:67777-220
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
LIGHT MINERAL OIL
Mineral Oil

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67777-220-02 28.35 in 1 TUBE
2 NDC:67777-220-03 14.17 in 1 TUBE
3 NDC:67777-220-04 113.4 in 1 TUBE
4 NDC:67777-220-07 425.3 in 1 JAR
5 NDC:67777-220-05 0.5 in 1 PACKET
6 NDC:67777-220-01 0.9 in 1 PACKET

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partB part333B 2009-12-01


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