NDC11 83027013801
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 |
|---|---|
| 83027-0138-01 | 83027-0138 |
| 83027-0138-1 | 83027-0138 |
| 83027-138-01 | 83027-138 |
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 (BOVINE), RHUS TOX, URTICA DIOICA, RHUS AROMATICA, RHUS GLABRA, HISTAMINUM HYDROCHLORICUM, RHUS DIVERSILOBA, ADRENOCORTICOTROPHIN | Nutritional Specialties, Inc. | ee799057-64c6-4e95-87ee-3f5020c9cf26 | 2024-07-24 | Warnings | 83027-0138-1 83027-0138 83027013801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.