NDC11 49580033406
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 |
|---|---|
| 49580-0334-06 | 49580-0334 |
| 49580-0334-6 | 49580-0334 |
| 49580-334-06 | 49580-334 |
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 |
|---|---|---|---|---|---|---|
| Mineral oil | MINERAL OIL | P & L Development, LLC | 68e88119-1468-4ab7-a5fa-242d960d25df | 2025-02-21 | Warnings | 49580-0334-6 49580-0334 49580033406 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.