Neomycin and Polymyxin B Sulfates and Bacitracin Zinc
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Neomycin and Polymyxin B Sulfates and Bacitracin Zinc
- Generic name
- NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND BACITRACIN ZINC
- Manufacturer
- Bausch & Lomb Incorporated
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- f3231f1c-665e-4efa-baa1-83bf296b2f8f
- SPL ID
- 2abff6dd-ac86-e766-e063-6394a90a9d70
- Version
- 14
- Effective date
- 2025-01-02
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:05
| Harmonized routes |
|---|
| OPHTHALMIC |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 064064 | derived:openfda.application_number |
| application number | ANDA064064 | openfda.application_number | |
| brand name | Neomycin and Polymyxin B Sulfates and Bacitracin Zinc | openfda.brand_name | |
| generic name | NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND BACITRACIN ZINC | openfda.generic_name | |
| manufacturer name | Bausch & Lomb Incorporated | openfda.manufacturer_name | |
| ndc | package | 24208-780-55 | openfda.package_ndc |
| ndc | product | 24208-780 | openfda.product_ndc |
| ndc11 | package | 24208078055 | derived:openfda.package_ndc |
| rxcui | 308493 | openfda.rxcui | |
| spl id | 2abff6dd-ac86-e766-e063-6394a90a9d70 | id | |
| spl set id | f3231f1c-665e-4efa-baa1-83bf296b2f8f | set_id | |
| unii | 89Y4M234ES | openfda.unii | |
| unii | 057Y626693 | openfda.unii | |
| unii | 19371312D4 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
WARNINGS NOT FOR INJECTION INTO THE EYE Neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment should never be directly introduced into the anterior chamber of the eye. Ophthalmic ointments may retard corneal wound healing. Topical antibiotics, particularly neomycin sulfate, may cause cutaneous sensitization. A precise incidence of hypersensitivity reactions (primarily skin rash) due to topical antibiotics is not known. The manifestations of sensitization to topical antibiotics are usually itching, reddening, and edema of the conjunctiva and eyelid. A sensitization reaction may manifest simply as a failure to heal. During long-term use of topical antibiotic products, periodic examination for such signs is advisable, and the patient should be told to discontinue the product if they are observed. Symptoms usually subside quickly on withdrawing the medication. Application of products containing these ingredients should be avoided for the patient thereafter ( see PRECAUTIONS: General ).
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS Adverse reactions have occurred with the anti-infective components of neomycin and polymyxin B sulfates and bacitracin zinc ophthalmic ointment. The exact incidence is not known. Reactions occurring most often are allergic sensitization reactions including itching, swelling, and conjunctival erythema ( see WARNINGS ). More serious hypersensitivity reactions, including anaphylaxis, have been reported rarely. Local irritation on instillation has also been reported. To report SUSPECTED ADVERSE REACTIONS, contact Bausch & Lomb Incorporated at 1-800-553-5340 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.