NDC11 50580061201
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 |
|---|---|
| 50580-0612-01 | 50580-0612 |
| 50580-0612-1 | 50580-0612 |
| 50580-612-01 | 50580-612 |
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 |
|---|---|---|---|---|---|---|
| Childrens Tylenol | ACETAMINOPHEN | Kenvue Brands LLC | babcb210-6a47-46ef-b4ea-bdde80411cd3 | 2024-11-08 | Warnings | 50580-612-01 50580061201 |
| Childrens TYLENOL | ACETAMINOPHEN | Kenvue Brands LLC | d8aa3b1a-5f63-49db-998c-35cd11bd733f | 2024-09-25 | Warnings | 50580-612-01 50580-612 50580061201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.