NDC11 49580039006
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 |
|---|---|
| 49580-0390-06 | 49580-0390 |
| 49580-0390-6 | 49580-0390 |
| 49580-390-06 | 49580-390 |
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 |
|---|---|---|---|---|---|---|
| Witch Hazel ReadyInCase | WITCH HAZEL | P & L Development, LLC | 1588244a-c9e8-4a04-b605-10e35c225e6c | 2025-02-12 | Warnings | 49580-0390-6 49580-0390 49580039006 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.