NDC11 43857060501
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 |
|---|---|
| 43857-0605-01 | 43857-0605 |
| 43857-0605-1 | 43857-0605 |
| 43857-605-01 | 43857-605 |
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 |
|---|---|---|---|---|---|---|
| Spineforce S-HP | ACONITUM NAPELLUS, AESCULUS HIPPOCASTANUM, COLCHICUM AUTUMNALE, HYPERICUM PERFORATUM, MAGNESIA PHOSPHORICA, PLUMBUM METALLICUM, RHUS TOX, ARNICA MONTANA | BioActive Nutritional, Inc. | 0ca4f64f-3c28-488b-bb48-ce8ab67951c8 | 2023-06-14 | Warnings | 43857-0605-1 43857-0605 43857060501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.