NDC product
Gencare-Senna-S Softgel
NDC 72090-054 · Pioneer Life Sciences, LLC
Key facts
| Product NDC | 72090-054 |
|---|---|
| Proprietary name | Gencare-Senna-S Softgel |
| Nonproprietary name | Sennosides 8.6 mg and Docusate Sodium 50 mg |
| Substances | DOCUSATE SODIUM, SENNOSIDES |
| Dosage form | CAPSULE, LIQUID FILLED |
| Route | ORAL |
| Labeler | Pioneer Life Sciences, LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | 505G(a)(3) |
| Marketing start | Jun 30, 2025 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: