NDC11 43857048101
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 |
|---|---|
| 43857-0481-01 | 43857-0481 |
| 43857-0481-1 | 43857-0481 |
| 43857-481-01 | 43857-481 |
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 |
|---|---|---|---|---|---|---|
| Free Radical | TRITICUM AESTIVUM, ALFALFA, FUCUS VESICULOSUS, LAMINARIA DIGITATA, NASTURTIUM AQUATICUM, ORYZA SATIVA, RAPHANUS SATIVUS, SYMPHYTUM OFFICINALE, HORDEUM VULGARE, ASPARAGUS OFFICINALIS, MANGANESE GLUCONATE, FERRUM PHOSPHORICUM, ARNICA MONTANA, CUPRUM METALLICUM, UBIDECARENONUM, ALPHA-KETOGLUTARICUM ACIDUM, GLYOXAL TRIMER DIHYDRATE, ALUMINUM METALLICUM, ANTIMONIUM CRUDUM, ARGENTUM METALLICUM, ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, BERYLLIUM METALLICUM, BISMUTHUM METALLICUM, BORON, BROMIUM | BioActive Nutritional, Inc. | e09f8fbb-e8c7-4c1b-994a-60f8fef79c0a | 2018-05-22 | Warnings | 43857-0481-1 43857-0481 43857048101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.