NDC 0081-0732 - Neosporin
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0081-0732
- Package NDCs from labels
- 0081-0732-86
- Manufacturer
- Burroughs Wellcome Inc.
- Effective date
- 2006-10-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Neosporin - Burroughs Wellcome Inc. | Burroughs Wellcome Inc. | 2006-10-03 | Human prescription drug label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0081-0732-86 | Neosporin | 3.5 g in 1 TUBE | OINTMENT | 3.5 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Neomycin and Polymyxin B Sulfates and Bacitracin Zinc | NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND BACITRACIN ZINC | Bausch & Lomb Incorporated | f3231f1c-665e-4efa-baa1-83bf296b2f8f | 2025-01-02 | Warnings, Adverse reactions | 308493 |
| 7E971C99-1F3F-4A9F-5084-FBE5B9F1A9E1 | 7E971C99-1F3F-4A9F-5084-FBE5B9F1A9E1 | 2006-10-03 | Warnings, Adverse reactions | 7E971C99-1F3F-4A9F-5084-FBE5B9F1A9E1 7E971C99-1F3F-4A9F-5084-FBE5B9F1A9E1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.