NDC11 37835022301
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 |
|---|---|
| 37835-0223-01 | 37835-0223 |
| 37835-0223-1 | 37835-0223 |
| 37835-223-01 | 37835-223 |
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 |
|---|---|---|---|---|---|---|
| STOOL SOFTENER | DOCUSATE SODIUM | Bi-Mart | 6589d373-0696-44c2-a9d4-a76e45526c5a | 2025-03-01 | Warnings | 37835-223-01 37835-223 37835022301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.