NDC11 64578009101
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 |
|---|---|
| 64578-0091-01 | 64578-0091 |
| 64578-0091-1 | 64578-0091 |
| 64578-091-01 | 64578-091 |
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 |
|---|---|---|---|---|---|---|
| Relax-Tone | CALCAREA CARBONICA, COFFEA CRUDA, HUMULUS LUPULUS, IGNATIA AMARA, KALI PHOSPHORICUM, MOSCHUS, NUX VOMICA, PASSIFLORA INCARNATE, PHOSPHORUS, PULSATILLA VULGARIS, STAPHYSAGRIA, VALERIANA OFFICINALIS | Energetix Corporation | 85563888-8097-4af4-8ab1-b6d6e545b499 | 2026-08-11 | Warnings | 64578-0091-1 64578-0091 64578009101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.