NDC11 43742195001
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 |
|---|---|
| 43742-1950-01 | 43742-1950 |
| 43742-1950-1 | 43742-1950 |
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 |
|---|---|---|---|---|---|---|
| Enviro I | POTASSIUM GLUCONATE, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, COFFEA TOSTA, THEA SINENSIS, CARBO VEGETABILIS, FERRUM IODATUM, FERRUM METALLICUM, GELSEMIUM SEMPERVIRENS, IODIUM, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, PULSATILLA (PRATENSIS), SELENIUM METALLICUM, ZINCUM METALLICUM, PEANUT, BLACK WALNUT, ENGLISH WALNUT, AMYGDALA AMARA, CASHEW, COCONUT, PECAN, BRAZIL NUT, TOMATO, SOLANUM TUBEROSUM, PIPER NIGRUM, EGGPLANT, RAPE SEED OIL, LINUM USITATISSIMUM, SESAME, SEED, CHEESE (STILTON), LAC VACCINUM, BEEF, | Deseret Biologicals, Inc. | 1de4f602-6e3c-4142-b60a-90585ac33884 | 2024-04-17 | Warnings | 43742-1950-1 43742-1950 43742195001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.