NDC11 51326080201
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 51326-0802-01 | 51326-0802 |
| 51326-0802-1 | 51326-0802 |
| 51326-802-01 | 51326-802 |
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 |
|---|---|---|---|---|---|---|
| Dr. Zenovia Spot Treatment | BENZOYL PEROXIDE | Topiderm, Inc. | dfdb3d8e-4d39-4ce4-851f-80b11972ca9e | 2024-06-11 | Warnings | 51326-802-01 51326-802 51326080201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.