Stool Softener with Stimulant Laxative

Product NDC: 59726-729
Requested package NDC: 59726-729-40
11-digit product format: 597260729
Labeler code: 59726
Product ID: 59726-729_fda67566-bfdb-4a03-a11d-6abb41a7a141
Type: HUMAN OTC DRUG
Nonproprietary name: docusate sodium and sennosides
Dosage form: TABLET
Route: ORAL
Labeler: P & L Development, LLC
Application: part334
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2018-09-30
Marketing end: 0000-00-00
Substance: DOCUSATE SODIUM; SENNOSIDES
Active strength: 50 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 2020-12-31
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	59726-729	59726-729-40	D	Discontinued by firm		2026-10-12

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 · 3 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Archive	Snapshot	Source SHA-256
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	59726-729	59726-729-40	I	Inactivated by FDA	excluded / ndc_excluded.zip	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	59726-729	59726-729-40	I	Inactivated by FDA	excluded / ndc_excluded.zip	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	59726-729	59726-729-40	I	Inactivated by FDA	excluded / ndc_excluded.zip	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59726-729-40	2023-04-20	C162847	48780-1	d6a99b39-6b59-a426-e053-dadaa90af4c2	Drug Facts
59726-729-40	2022-01-28	C162847	48780-1	d6a99b39-6b59-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59726-729	STOOL SOFTENER WITH STIMULANT LAXATIVE (DOCUSATE SODIUM AND SENNOSIDES) TABLET [P & L DEVELOPMENT, LLC]	3	Legacy NDC	20230421_a3db19b5-2f3e-4126-80eb-374c0ba51d2a.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F05Q2T2JA0	DOCUSATE SODIUM	577-11-7	DOCUSATE SODIUM
3FYP5M0IJX	SENNOSIDES		SENNOSIDES

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
59726-729-40	59726072940	400 TABLET in 1 BOTTLE, PLASTIC (59726-729-40)	400 tablet	2018-09-30	0000-00-00	No	No	Current