NDC11 43857064901
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 |
|---|---|
| 43857-0649-01 | 43857-0649 |
| 43857-0649-1 | 43857-0649 |
| 43857-649-01 | 43857-649 |
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 |
|---|---|---|---|---|---|---|
| Mold Mix Antigens | ARSENICUM ALBUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, ASPERGILLUS NIGER, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, TORULA CEREVISIAE, MUCOR RACEMOSUS, ALTERNARIA TENUIS NEES, CANDIDA KRUSEI, RHIZOPUS NIGRICANS | BioActive Nutritional, Inc. | 9c7be1b1-5f02-4178-b2fb-91912fe36221 | 2024-12-30 | Warnings | 43857-0649-1 43857-0649 43857064901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.