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Bacitracin Zinc by Dynarex Corporation

Dosage form: ointment
Ingredients: BACITRACIN ZINC 500[USP'U] in 1g
Labeler: Dynarex Corporation
NDC Code: 67777-220

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 Ointment

Active ingredient                                               Purpose
Bacitracin Zinc (500 Units in each gram)               First Aid 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

Stop use and ask a doctor if the condition persists or gets worse, or if a rash or other allergic reaction develops.

Indications & Usage:
  • in the eyes or over large areas of the body 
  • if you are allergic to any of the ingredients
  • 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, and burns.

Other information
  • store at controlled room temperature
  • Avoid excessive heat and humidity
  • Tamper Evident. Do not use if inner seal is torn, cut or open.

Ask a doctor if

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns.

Inactive ingredients

Hard Paraffin, Liquid Paraffin, White Soft Paraffin

Principal Display Panel

Dynarex Bacitracin Zinc Ointment:

1175 ESG.jpg

BACITRACIN ZINC 
bacitracin zinc ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-220
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (BACITRACIN) BACITRACIN500 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
LIGHT MINERAL OIL 
MINERAL OIL 
Packaging
#Item CodePackage Description
1NDC:67777-220-0228.35 g in 1 TUBE
2NDC:67777-220-0314.17 g in 1 TUBE
3NDC:67777-220-04113.4 g in 1 TUBE
4NDC:67777-220-07425.3 g in 1 JAR
5NDC:67777-220-050.5 g in 1 PACKET
6NDC:67777-220-010.9 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)
Establishment
NameAddressID/FEIOperations
Galentic Pharma (India) Pvt. Ltd.864201135manufacture(67777-220)
Establishment
NameAddressID/FEIOperations
Galentic Pharma (India) Private Limited650970176manufacture(67777-220)

 
Dynarex Corporation

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Medically reviewed on Jun 15, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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