Stimulant Laxative Plus
- Product NDC
- 50804-829
- Requested package NDC
- 50804-829-10
- 11-digit product format
- 508040829
- Labeler code
- 50804
- Product ID
- 50804-829_dae00c7b-f287-4cf9-bbf8-96785beb4bb8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate sodium, Sennosides
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Good Sense (Geiss, Destin & Dunn, Inc.)
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-12-31
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50804-829 | STIMULANT LAXATIVE PLUS STOOL SOFTENER (DOCUSATE SODIUM, SENNOSIDES) TABLET [GOOD SENSE (GEISS, DESTIN & DUNN, INC.)] | 3 | Legacy NDC | 20230212_23d3e1dd-0b9b-4dbb-84ef-0633986b81ad.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50804-829-10 | 50804082910 | 100 TABLET in 1 BOTTLE, PLASTIC (50804-829-10) | 100 tablet | 2018-12-31 | 0000-00-00 | No | No | Current |