NDC11 43742206001
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 |
|---|---|
| 43742-2060-01 | 43742-2060 |
| 43742-2060-1 | 43742-2060 |
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 |
|---|---|---|---|---|---|---|
| Systemic Detox | BOLDO, CHELIDONIUM MAJUS, SARSAPARILLA (SMILAX REGELII), GELSEMIUM SEMPERVIRENS, VERATRUM ALBUM,BETA VULGARIS, FERRUM METALLICUM, IODIUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PULSATILLA (PRATENSIS), SELENIUM METALLICUM, THUJA OCCIDENTALIS, ZINCUM METALLICUM | Deseret Biologicals, Inc. | a51b65c3-1cd2-4b97-96bc-6db1dbfaf82e | 2024-03-05 | Warnings | 43742-2060-1 43742-2060 43742206001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.