Stool Softener and Stimulant Laxative

Product NDC: 37808-549
11-digit product format: 378080549
Labeler code: 37808
Product ID: 37808-549_2e1460d5-2838-7eda-e063-6394a90a91d5
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate Sodium, Sennosides
Dosage form: TABLET
Route: ORAL
Labeler: H-E-B
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-02-04
Substance: DOCUSATE SODIUM; SENNOSIDES
Active strength: 50; 8.6 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	37808-549-29	I	Inactivated by FDA	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	37808-549-29	I	Inactivated by FDA	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	37808-549-29	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	37808-549-29	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	37808-549-29	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	37808-549-29	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	37808-549-29	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	37808-549-29	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	37808-549-29	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Stool Softener and Stimulant Laxative
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DOCUSATE SODIUM	50 mg/1
SENNOSIDES	8.6 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F05Q2T2JA0	Internal UNII lookup
3FYP5M0IJX	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
998740	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
c19280c2-f968-b582-e053-2995a90a9bd3	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
37808-549-29	2025-12-29	C162847	48780-1	2cef2736-7763-d83d-e063-dadaa90ab31f	HEB 209R Sennosides 8.6mg / Docusate Sodium 50mg 240ct
37808-549-29	2025-01-30	C162847	48780-1	2cef2736-7763-d83d-e063-dadaa90ab31f	HEB 209R Sennosides 8.6mg / Docusate Sodium 50mg 240ct

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
37808-549-29	Stool Softener and Stimulant Laxative	240 in 1 BOTTLE	TABLET	240		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-549	STOOL SOFTENER AND STIMULANT LAXATIVE (DOCUSATE SODIUM, SENNOSIDES) TABLET [H-E-B]	2	Current NDC, Legacy NDC, 1 package rows	20220205_c19280c2-f968-b582-e053-2995a90a9bd3.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 4 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Curewell Senna Syrup	SENNOSIDES	RMT HEALTH LLC	57345324-5140-5cde-e063-6294a90ab97c	2026-07-22	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE ORAL SOLUTION	WALGREEN COMPANY	4ffe54ae-3126-ba58-e063-6294a90a8877	2026-07-20	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Bryant Ranch Prepack	deca083b-5c72-40fa-9021-b74028426a5a	2026-07-20	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	Cardinal Health 107, LLC	fc5e82b6-e25c-4686-9781-2205819685f5	2026-07-20	Warnings	Exact identifier application number: M007
Best Choice Fiber Therapy Orange Flavor	PSYLLIUM HUSK	BEST CHOICE (VALU MERCHANDISERS COMPANY)	0b25f6c0-441b-41ef-ab19-2a29705a56c6	2026-07-17	Warnings	Exact identifier application number: M007
Best Choice Fiber Therapy original coarse	PSYLLIUM HUSK	BEST CHOICE (VALU MERCHANDISERS COMPANY)	d7eb71af-17e3-465e-b464-f77b3be7266d	2026-07-17	Warnings	Exact identifier application number: M007
Best Choice	CALCIUM POLYCARBOPHIL	BEST CHOICE (VALU MERCHANDISERS COMPANY)	24eb538f-abcb-4a91-b691-a8aac01c952a	2026-07-17	Warnings	Exact identifier application number: M007
Best Choice Fiber Laxative	PSYLLIUM HUSK	BEST CHOICE (VALU MERCHANDISERS COMPANY)	92b46689-b5fc-41f4-91ac-535699900b39	2026-07-17	Warnings	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	CVS Pharmacy, Inc.	498acb19-b2f4-4af0-8996-390115c17fe0	2026-07-17	Warnings, Adverse reactions	Exact identifier application number: M007
Best Choice Fiber Therapy	METHYLCELLULOSE	BEST CHOICE (VALU MERCHANDISERS COMPANY)	fab6567f-d988-43f2-a6cf-44e5b24af279	2026-07-17	Warnings	Exact identifier application number: M007
stool softener	DOCUSATE SODIUM	Amazon.com Services LLC	4f83953e-3779-43b7-a5c6-7442a0675d9b	2026-07-16	Warnings	Exact identifier application number: M007
Stool Softener Extra Strength	DOCUSATE SODIUM	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	183576bd-c252-471b-8797-32cac5b0329c	2026-07-16	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	Walgreens	3f9d54d9-a9d5-40ff-a8a2-431997b58999	2026-07-16	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Walgreens	7174021b-bdc0-4fd3-90e7-3904980033c4	2026-07-16	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	STRATEGIC SOURCING SERVICES LLC	ff2179bd-cc76-9ee9-e053-6294a90a01c9	2026-07-15	Warnings	Exact identifier application number: M007
FEVIA Constipation Control	DOCUSATE SODIUM	VIVUNT PHARMA LLC	4b21ca11-b81f-402c-e063-6394a90a3acb	2026-07-15	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	STRATEGIC SOURCING SERVICES LLC	56957a51-7366-f7ed-e063-6294a90abfc5	2026-07-14	Warnings	Exact identifier application number: M007
Laxative	SENNOSIDES	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	6103fded-622c-4551-9f32-ca1da44683ac	2026-07-10	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	The Kroger Co.	800fa966-077d-4624-9e36-75fe8863dad0	2026-07-10	Warnings	Exact identifier application number: M007
SENNA TIME	SENNOSIDES	Bryant Ranch Prepack	bdcf37fc-3938-4d3f-b669-35c6939eac4f	2026-07-10	Warnings	Exact identifier application number: M007

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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
998740	sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet	PSN	c19280c2-f968-b582-e053-2995a90a9bd3	3
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	c19280c2-f968-b582-e053-2995a90a9bd3	3
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	c19280c2-f968-b582-e053-2995a90a9bd3	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
37808-549-29	37808054929	240 TABLET in 1 BOTTLE (37808-549-29)	240 tablet	2022-05-04	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
HEB 209R Sennosides 8.6mg / Docusate Sodium 50mg 240ct	H-E-B \| TIME CAP LABORATORIES, INC.	2025-02-14	HUMAN OTC DRUG LABEL	3