Stool Softener
- Product NDC
- 30142-529
- 11-digit product format
- 301420529
- Labeler code
- 30142
- Product ID
- 30142-529_142401b0-c852-4256-9754-7c5f371f9570
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- docusate sodium and sennosides
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- The Kroger Co.
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-12-31
- Marketing end
- 2025-08-29
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 30142-529 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 30142-529 | 30142-529-60 | D | Discontinued by firm | 2026-10-15 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | 30142-529 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | ||
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 30142-529 | 30142-529-60 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 30142-529-60 | 30142052960 | 1 BOTTLE, PLASTIC in 1 BOX (30142-529-60) > 60 TABLET in 1 BOTTLE, PLASTIC | 2018-12-31 | 2025-08-29 | No | No | Current |