NDC11 43857049601
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 |
|---|---|
| 43857-0496-01 | 43857-0496 |
| 43857-0496-1 | 43857-0496 |
| 43857-496-01 | 43857-496 |
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 |
|---|---|---|---|---|---|---|
| Nightshade Antigen | CAPSICUM ANNUUM, SOLANUM TUBEROSUM, TABACUM, LYCOPERSICUM ESCULENTUM, SOLANUM MELONGENA, ALUMINUM METALLICUM, ARSENICUM ALBUM, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS) | BioActive Nutritional, Inc. | 47571afb-fa53-4c5b-ba35-8f0609a2bd75 | 2018-09-25 | Warnings | 43857-0496-1 43857-0496 43857049601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.