NDC11 70558000401
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 |
|---|---|
| 70558-0004-01 | 70558-0004 |
| 70558-0004-1 | 70558-0004 |
| 70558-004-01 | 70558-004 |
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 |
|---|---|---|---|---|---|---|
| Detox | BETA VULGARIS, BOLDO, CHELIDONIUM MAJUS, SARSAPARILLA (SMILAX REGELII), GELSEMIUM SEMPERVIRENS, VERATRUM ALBUM, FERRUM METALLICUM, IODIUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PULSATILLA (VULGARIS), SELENIUM METALLICUM, THUJA OCCIDENTALIS, ZINCUM METALLICUM | Pro Weight Loss Inc. | dbf87fe8-e7c4-4d6f-b55f-da23fcad355e | 2026-08-26 | Warnings | 70558-0004-1 70558-0004 70558000401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.