NDC11 43857062901
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 |
|---|---|
| 43857-0629-01 | 43857-0629 |
| 43857-0629-1 | 43857-0629 |
| 43857-629-01 | 43857-629 |
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 |
|---|---|---|---|---|---|---|
| Vitalizer | ECHINACEA (ANGUSTIFOLIA), IODIUM, ARSENICUM ALBUM, AURUM METALLICUM, CALCAREA FLUORICA, GALLICUM ACIDUM, HEKLA LAVA, NICCOLUM SULPHURICUM, PHOSPHORUS, SEDUM ACRE, SEMPERVIVUM TECTORUM, SENECIO AUREUS, BLATTA AMERICANA, ONOSMODIUM VIRGINIANUM | BioActive Nutritional, Inc. | a643abc6-5367-4b34-848a-83bdb6ddd87d | 2023-04-06 | Warnings | 43857-0629-1 43857-0629 43857062901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.