NDC11 59726087840
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 |
|---|---|
| 59726-0878-40 | 59726-0878 |
| 59726-878-40 | 59726-878 |
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 with Stimulant Laxative | DOCUSATE SODIUM AND SENNOSIDES | P & L Development, LLC | 0cbe3b61-ce35-4be1-9caf-9c61fce10ca2 | 2025-11-17 | Warnings | 59726-878-40 59726-878 59726087840 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.