NDC11 64578015401
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 |
|---|---|
| 64578-0154-01 | 64578-0154 |
| 64578-0154-1 | 64578-0154 |
| 64578-154-01 | 64578-154 |
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 |
|---|---|---|---|---|---|---|
| Sinus-Tone | ALLIUM CEPA, ECHINACEA, HYDRASTIS CANADENSIS, KALI BICHROMICUM, MERCURIUS SOLUBILIS, MERCURIUS SULPHURATUS RUBER, MUCOSA NASALIS SUIS, NATRUM SULPHURICUM, NUX MOSCHATA, PULSATILLA. | Energetix Corporation | e4dc6772-40c7-42af-8531-20b8d1883fb4 | 2026-08-11 | Warnings | 64578-0154-1 64578-0154 64578015401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.