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Name:Bacitracin Zinc
Manufacturer:Dynarex Corporation
Category:Over-the-counter (OTC) Marketed Drugs

Bacitracin Zinc

BACITRACIN ZINC  - bacitracin zinc ointment 
Dynarex Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.


Bacitracin Zinc

Active ingredient                   Purpose           
Bacitracin Zinc 500 Units                Antibactrerial


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 and serious burns
  • if the condition persists or gets worse
  • if a rash or any other allergic reaction develops

Other information

  • store at controlled room temperature 15°-30° C (59°-86° F)
  • Tamper Evident. Do not use if packet is torn, cut or opened.

Inactive ingredients

White Petrolatum

Indications and Usage

  • For first aid to help prevent infection in minor skin abrasions and rashes.


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

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center right away.

  • for external use only


Do not use:

Do not use:

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

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bacitracin zinc ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-239
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
# Item Code Package Description Multilevel Packaging
1 NDC:67777-239-01 12 BOX ( BOX) in 1 CASE contains a BOX
1 144 PACKET ( PACKET) in 1 BOX This package is contained within the CASE (67777-239-01) and contains a PACKET
1 0.9 g in 1 PACKET This package is contained within a BOX and a CASE (67777-239-01)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333B 12/01/2009

Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 03/2011 Dynarex Corporation

Reproduced with permission of U.S. National Library of Medicine

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