NDC11 81825001101
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 |
|---|---|
| 81825-0011-01 | 81825-0011 |
| 81825-0011-1 | 81825-0011 |
| 81825-011-01 | 81825-011 |
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 |
|---|---|---|---|---|---|---|
| Stress II | EPINEPHRINE, THYROID, UNSPECIFIED, BOS TAURUS PITUITARY GLAND, POSTERIOR, ARSENIC TRIOXIDE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, CONIUM MACULATUM FLOWERING TOP, CORTISONE ACETATE, CROTALUS HORRIDUS HORRIDUS VENOM, IRON, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PHOSPHORUS, SELENIUM, SEPIA OFFICINALIS JUICE, AND ZANTHOXYLUM AMERICANUM BARK | Zorex | 52dd7249-3ba5-4ed7-bce9-052fe3e28d10 | 2025-06-24 | Warnings | 81825-0011-1 81825-0011 81825001101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.