NDC11 43857056801
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 |
|---|---|
| 43857-0568-01 | 43857-0568 |
| 43857-0568-1 | 43857-0568 |
| 43857-568-01 | 43857-568 |
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 |
|---|---|---|---|---|---|---|
| Arterioforce II | BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), MYRRHA, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, TRIGONELLA FOENUM-GRAECUM, HYDRASTIS CANADENSIS, KALI IODATUM, ARNICA MONTANA, CACTUS GRANDIFLORUS, PROPOLIS, BARYTA CARBONICA, CONIUM MACULATUM, SECALE CORNUTUM | BioActive Nutritional, Inc. | ef98fbda-6815-4d0d-b07e-62ce420c4dee | 2026-08-11 | Warnings | 43857-0568-1 43857-0568 43857056801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.