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Bacitracin Package Insert

Updated:
Facts
Status:
Prescription (Rx)
Strength:
500 IU/g
Active ingredient:

Prescribing information (package insert) - Bacitracin

DESCRIPTION:

Each gram of ointment contains 500 units of Bacitracin in a low melting special base containing White Petrolatum and Mineral Oil.

ACTION:

The antibiotic, Bacitracin, exerts a profound action against many gram-positive pathogens, including the common Streptococci and Staphylococci. It is also destructive for certain gram-negative organisms. It is ineffective against fungi.

INDICATIONS:

For the treatment of superficial ocular infections involving the conjunctiva and/or cornea caused by Bacitracin susceptible organisms.

CONTRAINDICATIONS:

This product should not be used in patients with a history of hypersensitivity to Bacitracin.

PRECAUTIONS:

Bacitracin ophthalmic ointment should not be used in deep-seated ocular infections or in those that are likely to become systemic. The prolonged use of antibiotic containing preparations may result in overgrowth of nonsusceptible organisms particularly fungi. If new infections develop during treatment appropriate antibiotic or chemotherapy should be instituted.

ADVERSE REACTIONS:

Bacitracin has such a low incidence of allergenicity that for all practical purposes side reactions are practically non-existent. However, if such reaction should occur, therapy should be discontinued.

DOSAGE AND ADMINISTRATION:

The ointment should be applied directly into the conjunctival sac 1 to 3 times daily. In blepharitis all scales and crusts should be carefully removed and the ointment then spread uniformly over the lid margins. Patients should be instructed to take appropriate measures to avoid gross contamination of the ointment when applying the ointment directly to the infected eye.

HOW SUPPLIED:

3.5 g (1/8 Oz) sterile tamper proof tubes, NDC 42254-003-35.

Manufactured for:

Fera Pharmaceuticals, LLC

Locust Valley, NY 11560

FPBC00N Rev. 08/09

Repackaged by:

Rebel Distributors Corp

Thousand Oaks, CA 91320

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: ANDA 061212 · View the label on DailyMed

Revision date stated in the text: August 2009

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Drug information for Bacitracin

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Active ingredient Bacitracin 500 IU/g
Dosage form Ointment
Route Ophthalmic
Marketing status not in the current FDA NDC Directory
Company (applicant) PADAGIS US
FDA approval ANDA 061212Abbreviated New Drug Application (ANDA) – generic drug Approved November 9, 1971
Packages (NDC)
Package
500 IU/g – 3.5 g in 1 tube / 1 in 1 carton NDC 42254-003-35

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.