Home NDC 63868-874 Stool Softener plus Laxative
Product NDC 63868-874
11-digit product format 638680874
Labeler code 63868
Product ID 63868-874_1da9a202-6cae-4361-8298-6c0e086f53b3
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium Sennosides
Dosage form TABLET
Route ORAL
Labeler QUALITY CHOICE (Chain Drug Marketing Association)
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2019-01-31
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 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 63868-874-60 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 63868-874-60 f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 63868-874-60 63868087460 1 BOTTLE, PLASTIC in 1 BOX (63868-874-60) > 60 TABLET in 1 BOTTLE, PLASTIC 2019-01-31 0000-00-00 No No Current