FDA.reportPublic FDA data

Stool Softener Laxative

Product NDC
11822-2039
11-digit product format
118222039
Labeler code
11822
Product ID
11822-2039_6923fa14-5482-421d-acfa-21f3b3d1db02
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Rite Aid Corporation
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2021-04-30
Marketing end
0000-00-00
Substance
DOCUSATE SODIUM
Active strength
100 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct11822-2039DDiscontinued by firm2026-09-14
excluded packagepackage11822-203911822-2039-6DDiscontinued by firm2026-09-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-2039STOOL SOFTENER LAXATIVE (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [RITE AID CORPORATION]4Legacy NDC20240509_6cc4d42e-b2b6-4171-8ff3-60297f398e7b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11822-2039-611822203906250 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (11822-2039-6) 2021-04-300000-00-00NoNoCurrent