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 20 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
up and up fiber therapy	PSYLLIUM HUSK	Target Corporation	674753ee-1174-4c06-9ed3-a090b338a39e	2025-11-05	Warnings	Exact identifier application number: M007
up and up fiber therapy	PSYLLIUM HUSK	TARGET CORPORATION	956c48f8-c705-4a86-9866-c68a48ddeb6c	2025-11-05	Warnings	Exact identifier application number: M007
CEO-TWO	LAXATIVE	Beutlich Pharmaceuticals, LLC	08670636-5795-4db0-e063-6294a90afa4b	2025-11-05	Warnings	Exact identifier application number: M007
up and up gentle laxative	BISACODYL	Target Corporation	4a29dc2b-b68f-471b-a84e-4a5096aa3748	2025-11-04	Warnings	Exact identifier application number: M007
Target Fiber Laxative	PSYLLIUM HUSK	TARGET CORPORATION	a581116a-392d-4ac3-ae15-4318506a7b2a	2025-11-04	Warnings	Exact identifier application number: M007
up and up fiber therapy	CALCIUM POLYCARBOPHIL	Target Corporation.	e5473950-06f4-4ea4-975b-3ac94957e776	2025-11-04	Warnings	Exact identifier application number: M007
up and up fiber therapy Natural Fiber	PSYLLIUM HUSK	Target Corporation	f8b1c831-6fd0-4a58-9726-4e0f986c8084	2025-11-04	Warnings	Exact identifier application number: M007
OneLAX	BISACODYL	AKRON PHARMA INC	be4eeb4d-df29-45dc-94ff-933e52c8b6f6	2025-11-03	Warnings	Exact identifier application number: M007
Gentle Stool Softener	DOCUSATE SODIUM	WALGREEN COMPANY	169b33f9-e559-47bf-bbba-c7eda4762c7f	2025-10-31	Warnings	Exact identifier application number: M007
Senna S	DOCUSATE SODIUM, SENNOSIDES	Walgreens	765bfd9b-7a21-4315-9add-cf13007722d5	2025-10-31	Warnings	Exact identifier application number: M007
Gentle Stool Softener	DOCUSATE SODIUM	WALGREEN COMPANY	71b15339-2585-4fae-8445-6fbb4f0a378e	2025-10-31	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Major Pharmaceuticals	97561cd4-63d9-44c2-a3a3-ec668a09a4ed	2025-10-31	Warnings	Exact identifier application number: M007
Fiber Caplets	CALCIUM POLYCARBOPHIL	SAFEWAY	08e2e8b0-90b3-48d6-a72a-40688c74771a	2025-10-29	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN	Chain Drug Marketing Association Inc.	424d91f0-ecf9-6d9b-e063-6394a90a8006	2025-10-29	Warnings	Exact identifier application number: M007
Publix Laxative Maximum Strength	CALCIUM SENNOSIDES	PUBLIX SUPER MARKETS, INC	11112859-ef1e-4b37-9915-ba4d06a3f198	2025-10-28	Warnings	Exact identifier application number: M007
Publix Stimulant Laxative	BISACODYL	PUBLIX SUPER MARKETS, INC	02e596a7-b8e5-4f55-9bc6-6d17e0fabda7	2025-10-28	Warnings	Exact identifier application number: M007
PUBLIX	PSYLLIUM HUSK	PUBLIX SUPER MARKETS, INC	55f98d3f-f282-4f19-b373-0b59640d274d	2025-10-28	Warnings	Exact identifier application number: M007
PUBLIX	CALCIUM POLYCARBOPHIL	PUBLIX SUPER MARKETS, INC	02e3f4ce-8961-425c-98a9-3b9d66709ca5	2025-10-28	Warnings	Exact identifier application number: M007
Publix Women Laxative	BISACODYL	PUBLIX SUPER MARKETS, INC	03eeca55-f239-4a01-a900-c1943f27a834	2025-10-28	Warnings	Exact identifier application number: M007
Publix Fiber Therapy Orange Smooth	PSYLLIUM HUSK	PUBLIX SUPER MARKETS, INC	b9c54c20-cd82-4627-9217-a66834db4799	2025-10-28	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