NDC11 87708000204
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 |
|---|---|
| 87708-0002-04 | 87708-0002 |
| 87708-0002-4 | 87708-0002 |
| 87708-002-04 | 87708-002 |
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 |
|---|---|---|---|---|---|---|
| RENUEVO ANTI-DAMDRUFF | ZINC PYRITHIONE | LEON UP GLOBAL HOLDING CORP | 5387b840-ad0a-4c20-e063-6294a90a59e3 | 2026-06-05 | Warnings | 87708-002-04 87708-002 87708000204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.