warnings
WARNINGS Ophthalmic ointments may retard corneal healing.
Bacitracin Zinc and Polymyxin B Sulfate
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
- Bacitracin Zinc and Polymyxin B Sulfate
- Generic name
- BACITRACIN ZINC AND POLYMYXIN B SULFATE
- Manufacturer
- A-S Medication Solutions
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 51f6eac3-205e-4beb-8522-6ba2c593f350
- SPL ID
- f616c4bc-ebe1-4cf6-a22b-8f44773bc0d1
- Version
- 16
- Effective date
- 2026-03-17
- Source export date
- 2026-10-27
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/d7629e6f844435cfe6cb0cf8c5341c46775ea16c5af42c77a22a2ffe820a2cd2/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 19:50:13
| 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 | 064046 | derived:openfda.application_number |
| application number | ANDA064046 | openfda.application_number | |
| brand name | Bacitracin Zinc and Polymyxin B Sulfate | openfda.brand_name | |
| generic name | BACITRACIN ZINC AND POLYMYXIN B SULFATE | openfda.generic_name | |
| manufacturer name | A-S Medication Solutions | openfda.manufacturer_name | |
| ndc | package | 50090-3274-0 | openfda.package_ndc |
| ndc | product | 50090-3274 | openfda.product_ndc |
| ndc11 | package | 50090327400 | derived:openfda.package_ndc |
| rxcui | 308511 | openfda.rxcui | |
| spl id | f616c4bc-ebe1-4cf6-a22b-8f44773bc0d1 | id | |
| spl set id | 51f6eac3-205e-4beb-8522-6ba2c593f350 | set_id | |
| unii | 89Y4M234ES | openfda.unii | |
| unii | 19371312D4 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS 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.