NDC11 84878019904
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 |
|---|---|
| 84878-0199-04 | 84878-0199 |
| 84878-0199-4 | 84878-0199 |
| 84878-199-04 | 84878-199 |
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 |
|---|---|---|---|---|---|---|
| Sunsolve MD Firm and Replenish | ZINC OXIDE | Sunsolve MD Inc | 26f3417b-9ea4-e577-e063-6294a90ae53c | 2025-11-14 | Warnings | 84878-199-04 84878-199 84878019904 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.