NDC11 43857057001
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 |
|---|---|
| 43857-0570-01 | 43857-0570 |
| 43857-0570-1 | 43857-0570 |
| 43857-570-01 | 43857-570 |
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 |
|---|---|---|---|---|---|---|
| Epiforce E | LAPPA MAJOR, PHYTOLACCA DECANDRA, TRIFOLIUM PRATENSE, HYDROCOTYLE ASIATICA, ARSENICUM ALBUM, GRAPHITES, MEZEREUM | BioActive Nutritional, Inc. | ebec32bd-9df0-4a13-b47f-d0caa5f7c9e3 | 2026-03-05 | Warnings | 43857-0570-1 43857-0570 43857057001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.