FDA.reportPublic FDA data

Laxative Stool Softener

Product NDC
69842-830
11-digit product format
698420830
Labeler code
69842
Product ID
69842-830_b948580e-f61b-4555-a482-3f0a0d7fb4ca
Type
HUMAN OTC DRUG
Nonproprietary name
DOCUSATE SODIUM, SENNOSIDES
Dosage form
TABLET
Route
ORAL
Labeler
CVS Pharmacy
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-05-01
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 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct69842-830DDiscontinued by firm2026-10-05
excluded packagepackage69842-83069842-830-18DDiscontinued by firm2026-10-05
excluded packagepackage69842-83069842-830-30DDiscontinued by firm2026-10-05

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 · 6 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage69842-830-30d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage69842-830-18d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage69842-830-30f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage69842-830-18f5e01cc5f278…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
69842-830-182020-10-27Drug Facts
69842-830-302020-10-27Drug Facts
69842-830-182020-09-27Drug Facts
69842-830-302020-09-27Drug Facts
69842-830-182020-09-25Drug Facts
69842-830-302020-09-25Drug Facts
69842-830-182020-07-22Drug Facts
69842-830-302020-07-22Drug Facts

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-830-1869842083018180 TABLET in 1 BOTTLE, PLASTIC (69842-830-18) 180 tablet2019-05-010000-00-00NoNoCurrent
69842-830-30698420830301 BOTTLE, PLASTIC in 1 BOX (69842-830-30) > 30 TABLET in 1 BOTTLE, PLASTIC2019-05-010000-00-00NoNoCurrent