NDC11 43742214101
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 |
|---|---|
| 43742-2141-01 | 43742-2141 |
| 43742-2141-1 | 43742-2141 |
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 | BETA VULGARIS, BOLDO, CHELIDONIUM MAJUS, FERRUM METALLICUM, GELSEMIUM SEMPERVIRENS, IODIUM, LYCOPODIUM CLAVATUM, NUX VOMICA, PULSATILLA (PRATENSIS), SARSAPARILLA (SMILAX REGELII), SELENIUM METALLICUM, THUJA OCCIDENTALIS, VERATRUM ALBUM, ZINCUM METALLICUM | Deseret Biologicals, Inc. | 7ef75c3f-2d34-4822-8b94-8bce88709afd | 2024-03-13 | Warnings | 43742-2141-1 43742-2141 43742214101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.