NDC11 63621033514
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 |
|---|---|
| 63621-0335-14 | 63621-0335 |
| 63621-335-14 | 63621-335 |
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 |
|---|---|---|---|---|---|---|
| Prestige | CHLOROXYLENOL | Sunburst Chemicals, Inc. | 2e4bb97c-9c16-43d1-aea3-54723c7afc45 | 2024-03-21 | Warnings | 63621-335-14 63621-335 63621033514 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.