NDC11 43857021701
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 |
|---|---|
| 43857-0217-01 | 43857-0217 |
| 43857-0217-1 | 43857-0217 |
| 43857-217-01 | 43857-217 |
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 |
|---|---|---|---|---|---|---|
| Enuresis | EQUISETUM HYEMALE, SOLIDAGO VIRGAUREA, UVA-URSI, ARGENTUM METALLICUM, CAUSTICUM, KREOSOTUM, NITRICUM ACIDUM, SEPIA, THUJA OCCIDENTALIS | BioActive Nutritional, Inc. | 22105dde-b570-4af6-a7b8-e942f649e934 | 2017-06-14 | Warnings | 43857-0217-1 43857-0217 43857021701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.