NDC11 83027003901
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 |
|---|---|
| 83027-0039-01 | 83027-0039 |
| 83027-0039-1 | 83027-0039 |
| 83027-039-01 | 83027-039 |
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 |
|---|---|---|---|---|---|---|
| Poison Ivy and Oak Formula | GLANDULA SUPRARENALIS (BOVINE), HEPAR SUIS, RHUS TOX, URTICA DIOICA, RHUS AROMATICA, RHUS GLABRA, HISTAMINUM HYDROCHLORICUM, RHUS DIVERSILOBA, ADRENOCORTICOTROPHIN | Nutritional Specialties, Inc. | b906ec41-4049-43df-9ef3-ea71225cc910 | 2024-07-25 | Warnings | 83027-0039-1 83027-0039 83027003901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.