NDC11 84878020002
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 |
|---|---|
| 84878-0200-02 | 84878-0200 |
| 84878-0200-2 | 84878-0200 |
| 84878-200-02 | 84878-200 |
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 Correct and Fade | ZINC OXIDE | Sunsolve MD Inc | 26f3ad9f-f8ca-05d4-e063-6394a90ad5c4 | 2025-11-14 | Warnings | 84878-200-02 84878-200 84878020002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.