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Bacitracin by Dynarex Corporation

Medically reviewed on May 7, 2018

Dosage form: ointment
Ingredients: BACITRACIN 500[iU] in 1g
Labeler: Dynarex Corporation
NDC Code: 67777-219

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.

1162_1163_Bacitracin_Ointment

Active ingredient               Purpose
Bacitracin 500 Units                Antibiotic

Warnings:

For external use only

Dosage and 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.

Do not use:
  • 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

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

Indications and Usage

Ask a doctor before use:

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

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

Inactive ingredients

Light Mineral Oil, White Petrolatum

Principal Display Panel

Bacitracin Ointment:

bacitracin-galentic-ointment-01.jpg

BACITRACIN 
bacitracin ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-219
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN (BACITRACIN ) BACITRACIN 500 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL 
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:67777-219-0172 TUBE (TUBE) in 1 CASE
128.35 g in 1 TUBE
2NDC:67777-219-0472 TUBE (TUBE) in 1 CASE
214.17 g in 1 TUBE
3NDC:67777-219-0612 BOX (BOX) in 1 CASE
3144 PACKET (PACKET) in 1 BOX
30.5 g in 1 PACKET
4NDC:67777-219-0712 BOX (BOX) in 1 CASE
4144 PACKET (PACKET) in 1 BOX
40.9 g in 1 PACKET
5NDC:67777-219-0572 TUBE (TUBE) in 1 CASE
556.7 g in 1 TUBE
6NDC:67777-219-0272 TUBE (TUBE) in 1 CASE
6113.4 g in 1 TUBE
7NDC:67777-219-0312 JAR (JAR) in 1 CASE
7425.3 g in 1 JAR
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)

 
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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