NDC11 00135061601
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 |
|---|---|
| 00135-0616-01 | 00135-0616 |
| 00135-0616-1 | 00135-0616 |
| 00135-616-01 | 00135-616 |
| 0135-0616-01 | 0135-0616 |
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 |
|---|---|---|---|---|---|---|
| FLONASE SENSIMIST ALLERGY RELIEF | FLUTICASONE FUROATE | Haleon US Holdings LLC | 893234b5-be82-4425-b850-2b884637b18e | 2024-03-05 | Warnings | 0135-0616-01 0135-0616 00135061601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.