NDC11 43857041301
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 |
|---|---|
| 43857-0413-01 | 43857-0413 |
| 43857-0413-1 | 43857-0413 |
| 43857-413-01 | 43857-413 |
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 HP | ARGENTUM NITRICUM, BELLADONNA, CAUSTICUM, EQUISETUM HYEMALE, KREOSOTUM, NITRICUM ACIDUM, PULSATILLA (VULGARIS), THUJA OCCIDENTALIS | BioActive Nutritional, Inc. | a6fff9be-e78d-4539-b741-6a8080a164a0 | 2016-09-07 | Warnings | 43857-0413-1 43857-0413 43857041301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.