NDC11 71742000801
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 |
|---|---|
| 71742-0008-01 | 71742-0008 |
| 71742-0008-1 | 71742-0008 |
| 71742-008-01 | 71742-008 |
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 |
|---|---|---|---|---|---|---|
| Heavy Metal Detox T014 | ALLIUM SATIVUM, AVENA SATIVA, BERBERIS VULGARIS, LAPPA MAJOR, PHYTOLACCA DECANDRA, SOLIDAGO VIRGAUREA, LYCOPODIUM CLAVATUM, NUX VOMICA, ALUMINUM METALLICUM, ANTIMONIUM CRUDUM, ARGENTUM METALLICUM, ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, BERYLLIUM METALLICUM, BISMUTHUM METALLICUM, BORON, BROMIUM, CADMIUM METALLICUM, CERIUM METALLICUM, CESIUM CHLORIDE, CHROMIUM, COBALTUM METALLICUM, CUPRUM METALLICUM, DYSPROSIUM METALLICUM, ERBIUM METALLICUM, EUROPIUM METALLICUM, FERRUM METALLICUM | Guangzhou Renuma Medical Systems Co., Ltd | 41ce8009-71f2-418c-a38d-0cfaccfb74b4 | 2017-10-26 | Warnings | 71742-0008-1 71742-0008 71742000801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.