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 40 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Milk of Magnesia mint	MAGNESIUM HYDROXIDE	Meijer, Inc.	bb8ba371-f53c-1088-e053-2a95a90a4cbf	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	STRATEGIC SOURCING SERVICES LLC	00c61622-367b-0a5b-e063-6294a90a6706	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Strategic Sourcing Services LLC	003a3c0d-7a48-e44d-e063-6394a90a3f4a	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	Geri-Care Pharmaceuticals, Corp	2d1be236-e136-4727-a52d-714f62880088	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	AMERISOURCEBERGEN DRUG CORPORATION	5d690d82-e4fb-57ad-e053-2a91aa0a38ea	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	AMERISOURCEBERGEN DRUG CORPORATION	5d6a8048-93e7-42e5-e053-2991aa0acabd	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	AMERISOURCEBERGEN DRUG CORPORATION	5d7f5a38-4222-5bfb-e053-2991aa0a17e3	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	CARDINAL HEALTH	af4b6b64-97c9-a794-e053-2a95a90aaf0b	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	CARDINAL HEALTH	af5ddf5d-b1f5-2918-e053-2995a90a2d61	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	H E B	ab998776-6b30-9f17-e053-2995a90a96cd	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	H E B	abfe89c8-86f1-bd1e-e053-2995a90af773	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	GOODSENSE	a951617d-c6fa-75e0-e053-2995a90afcf8	2023-11-07	Warnings	Exact identifier application number: M007
Milk of Magnesia	MAGNESIUM HYDROXIDE	KROGER COMPANY	a1b04366-ff67-3bb3-e053-2a95a90a816c	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	BETTER LIVING BRANDS, LLC	b9440381-df40-4bc7-e053-2995a90ae83f	2023-11-07	Warnings	Exact identifier application number: M007
Milk of Magnesia mint	MAGNESIUM HYDROXIDE	TOP CARE (TOPCO ASSOCIATES LLC)	b83f6027-51a0-1730-e053-2995a90a553b	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	TOP CARE (TOPCO ASSOCIATES LLC)	b83eb807-d522-4408-e053-2a95a90a7926	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	TOP CARE (TOPCO ASSOCIATES LLC)	b83f0c1c-0e90-2888-e053-2995a90a0b96	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	DOLGENCORP, INC.	b6991abf-9819-701c-e053-2a95a90ac0b4	2023-11-07	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	Chain Drug Marketing Association	7722145c-913c-4ed5-a9b2-a6c343064066	2023-11-06	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	Chain Drug Marketing Association	12361478-d178-4950-9458-4e2e56565599	2023-11-06	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