FDA.reportPublic FDA data

Stool Softener

Product NDC
69842-829
Requested package NDC
69842-829-25
11-digit product format
698420829
Labeler code
69842
Product ID
69842-829_d9285c9c-ec11-487a-9b4d-c42dad19ca8e
Type
HUMAN OTC DRUG
Nonproprietary name
docusate sodium and sennosides
Dosage form
TABLET
Route
ORAL
Labeler
CVS Pharmacy
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-04-30
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

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.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage69842-82969842-829-25DDiscontinued by firm2026-10-12

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.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage69842-82969842-829-25DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage69842-82969842-829-25DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
69842-829-102020-10-27Drug Facts
69842-829-252020-10-27Drug Facts
69842-829-402020-10-27Drug Facts
69842-829-102020-09-27Drug Facts
69842-829-252020-09-27Drug Facts
69842-829-402020-09-27Drug Facts
69842-829-102020-09-25Drug Facts
69842-829-252020-09-25Drug Facts
69842-829-402020-09-25Drug Facts
69842-829-102020-07-22Drug Facts
69842-829-252020-07-22Drug Facts
69842-829-402020-07-22Drug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69842-829-40EA - Each69842-8299584ac5d-6e22-45df-8989-c1d638a26ede12021-02-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-829-2569842082925250 TABLET in 1 BOTTLE, PLASTIC (69842-829-25) 250 tablet2019-04-300000-00-00NoNoCurrent