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Bacitracin by Kinray Inc.

Medically reviewed on March 6, 2018

Dosage form: ointment
Ingredients: BACITRACIN 500[iU] in 1g
Labeler: Kinray Inc.
NDC Code: 61715-079

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 Ointment

Active ingredient                        Purpose
Bacitracin Zinc 500 Units                Antibiotic

Purpose:

First aid to help prevent infection.

Warnings:

For external use only

Dosage and Administration

Directions:

  • clean the affected areas
  • apply a small amount of product (an amountb 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

Indications and Usage

First aid to help prevent infection in:

  • minor cuts
  • scrapes
  • burns

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:
  • 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

Ask a doctor before use:
  • in case of deep or puncture wounds
  • animal bites
  • serious burns

Keep out of reach of children
  • If swallowed, get medical help or contact a Poison Control Center right away

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

Inactive ingredients

Light Mineral Oil, White Petrolatum

Principal Display Panel

Kinray Bacitracin Ointment:

KR1163 Bacitracin.jpg

BACITRACIN 
bacitracin ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61715-079
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN (BACITRACIN) BACITRACIN500 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL 
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:61715-079-0128.35 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B08/02/2013
Labeler - Kinray Inc. (012574513)
Registrant - Dynarex Corporation (008124539)

 
Kinray Inc.

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Further information

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

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