DOCUZEN

Product NDC: 71574-700
11-digit product format: 715740700
Labeler code: 71574
Product ID: 71574-700_bf899923-8769-4738-88ea-b1a07997b959
Type: HUMAN OTC DRUG
Nonproprietary name: Sennosides 8.6mg and Docusate Sodium 50mg
Dosage form: TABLET
Route: ORAL
Labeler: Village Pharma
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2018-11-27
Substance: SENNOSIDES; DOCUSATE SODIUM
Active strength: 8.6; 50 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 2027-12-31
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 · 20 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
2025-04-01 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	71574-700-60	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	71574-700-60	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	71574-700-60	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	71574-700-60	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	71574-700-60	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	71574-700-60	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	71574-700-60	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	71574-700-60	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	71574-700-60	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	71574-700-60	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

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: DOCUZEN
Listing expiration: 2027-12-31

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3FYP5M0IJX	Internal UNII lookup
F05Q2T2JA0	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
29102014-9b0e-4899-958d-83111f94a612	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
c6f86816-7da6-43ea-8c25-ac9758311cc5	Product name	1	20220118
252e11b6-1a9a-4283-a242-df2c129c496d	Product name	3	20170717

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2025-06-11	Drug Facts
2025-01-30	Drug Facts
2023-11-10	Drug Facts
2022-01-28	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71574-700-60	DOCUZEN	60 in 1 BOTTLE, PLASTIC	TABLET	60		3

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71574-700-60	EA - Each	71574-700	663e7d7f-3f91-4d2c-8cff-71d91c953930	1	2019-01-24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71574-700	DOCUZEN (SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG) TABLET [VILLAGE PHARMA]	2	Current NDC, Legacy NDC, 1 package rows	20231111_29102014-9b0e-4899-958d-83111f94a612.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 8 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Laxomil	BISACODYL 5MG	Pharmadel LLC	3999935b-d8e8-52a6-e063-6294a90aa2a2	2026-03-20	Warnings	Exact identifier application number: M007
Laxative Enteric Coated	BISACODYL 5MG	Grocery Outlet	c820e6a1-fa23-447a-9ee9-50a1bd617adb	2026-03-19	Warnings	Exact identifier application number: M007
CITRUCEL	METHYLCELLULOSE	Haleon US Holdings LLC	9d5f2244-a610-4d45-b6e8-e79bb17a558f	2026-03-18	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Safeway, Inc.	f178b31d-4843-4b91-a0d5-ab5ade835dc2	2026-03-16	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Safeway, Inc.	12ab9c3c-1f4b-43cd-83ac-b5f80b1aa54c	2026-03-13	Warnings	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Old East Main Co.	a1ca668a-3bf9-46a9-8a4f-5cb61547bb81	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Vi-Jon, LLC	b29775df-8470-4fe3-bee3-f0490ea6903f	2026-03-12	Warnings	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Nice-Pak Products, LLC	cc43d514-ee82-4314-99b2-c64380f98779	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M007
Fibercon	CALCIUM POLYCARBOPHIL	Foundation Consumer Brands	7992a4bb-5535-4a1d-867d-a99f7e0c1be7	2026-03-12	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Walgreens	cda27a9c-9175-4b07-9c0b-d8d897882965	2026-03-12	Warnings	Exact identifier application number: M007
Magnesium Citrate Saline Laxative - Lemon Flavor	MAGNESIUM CITRATE	Universal Distribution Center LLC	aa02c9af-22b8-4ec2-9e43-fe073f5e617b	2026-03-11	Warnings	Exact identifier application number: M007
Magnesium Citrate Saline Laxative - Grape Flavor	MAGNESIUM CITRATE	Universal Distribution Center LLC	021ebb61-2466-4272-8f7d-b49cafd08754	2026-03-11	Warnings	Exact identifier application number: M007
Magnesium Citrate Saline Laxative - Cherry Flavor	MAGNESIUM CITRATE	Universal Distribution Center LLC	1f14411b-6833-40e6-b1a5-2b8c5bf709d3	2026-03-11	Warnings	Exact identifier application number: M007
Citroma	MAGNESIUM CITRATE	UpLift Brands, LLC	f83ba007-734d-4910-87cb-02e45285e161	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M007
Citroma	MAGNESIUM CITRATE	UpLift Brands, LLC	57e914fa-8fa2-4221-bb5f-534f0ea0aba7	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M007
Citroma	MAGNESIUM CITRATE	UpLift Brands, LLC	f28a9043-e0ee-4b38-95d9-d3f23d400691	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	Amerisource Bergen	4caf0bcb-c1bf-0ae7-e063-6294a90a344b	2026-03-10	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Walgreens	92df761b-da68-4ce9-b02a-a5a74fd6620e	2026-03-10	Warnings	Exact identifier application number: M007
Fleet	GLYCERIN	C.B. Fleet Company, Inc.	31778652-e60e-4098-8e90-3e4f56b5800c	2026-03-06	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN	Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd	4c6094b7-c1ef-26a3-e063-6394a90af4cc	2026-03-06	Warnings	Exact identifier application number: M007

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

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	92879e62-f60a-4ab4-9532-610cdd2628ee	5
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	92879e62-f60a-4ab4-9532-610cdd2628ee	5
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	92879e62-f60a-4ab4-9532-610cdd2628ee	5
998740	sennosides 8.6 MG / docusate sodium 50 MG Oral Tablet	PSN	29102014-9b0e-4899-958d-83111f94a612	3
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	29102014-9b0e-4899-958d-83111f94a612	3
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	29102014-9b0e-4899-958d-83111f94a612	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71574-700-60	71574070060	60 TABLET in 1 BOTTLE, PLASTIC (71574-700-60)	60 tablet	2018-11-27	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	Village Pharma \| Pharbest Pharmaceuticals, Inc.	2025-06-01	HUMAN OTC DRUG LABEL	3
Drug Facts	Proficient Rx LP	2023-11-01	HUMAN OTC DRUG LABEL	5