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Bacitracin Zinc by Dynarex Corporation

Dosage form: ointment
Ingredients: BACITRACIN ZINC 500[iU] in 1g
Labeler: Dynarex Corporation
NDC Code: 67777-239

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

Uses: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.

Directions:
  • 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

Principal Display Panel

Principal Display Panel

BACITRACIN ZINC 
bacitracin zinc ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-239
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (BACITRACIN ZINC) BACITRACIN ZINC500 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:67777-239-0112 BOX (BOX) in 1 CASE
1144 PACKET (PACKET) in 1 BOX
10.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B12/01/2009
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 03/2011
 
Dynarex Corporation

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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