NDC11 83027000101
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 |
|---|---|
| 83027-0001-01 | 83027-0001 |
| 83027-0001-1 | 83027-0001 |
| 83027-001-01 | 83027-001 |
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 |
|---|---|---|---|---|---|---|
| Dizzy Formula | ARNICA MONTANA, HYDROCOTYLE ASIATICA, AMBRA GRISEA, ARGENTUM NITRICUM, COCCULUS INDICUS, CONIUM MACULATUM, LAC CANINUM, THERIDION | Nutritional Specialties, Inc. | aaccfd13-6559-4976-90d1-aa3b4a4a79db | 2026-03-31 | Warnings | 83027-0001-1 83027-0001 83027000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.