NDC11 27281004965
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 |
|---|---|
| 27281-0049-65 | 27281-0049 |
| 27281-049-65 | 27281-049 |
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 |
|---|---|---|---|---|---|---|
| Immune Booster | APIS MELLIFICA, BAPTISIA TINCTORIA, CARDUUS MARIANUS, ECHINACEA ANGUSTIFOLIA, GALLUM APARINE, MERCURIUS CORROSIVUS, MERCURIUS SULPHURATUS RUBER, NITRICUM ACIDUM, SULPHUR IODATUM, THUJA OCCIDENTALIS. | Sunway Biotech LLC | 9ae14a66-9f6b-4ca8-b335-f6f75ddb8d93 | 2021-12-29 | Warnings | 27281-049-65 27281-049 27281004965 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.