Senna-S

Product NDC: 73057-378
11-digit product format: 730570378
Labeler code: 73057
Product ID: 73057-378_2c270be1-981f-3019-e063-6394a90a098f
Type: HUMAN OTC DRUG
Nonproprietary name: Sennosides 8.6mg and Docusate Sodium 50mg
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Ulai Health LLC
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2019-07-10
Substance: SENNOSIDES; DOCUSATE SODIUM
Active strength: 8.6; 50 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 · 8 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73057-378-11	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73057-378-08	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	73057-378-07	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73057-378-11	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73057-378-08	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	73057-378-07	`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: Senna-S
Listing expiration: 2026-12-31

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
c0e27b02-8ef2-4239-8f8c-790f7d978dc0	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
73057-378-07	2022-01-31	Drug Facts
73057-378-08	2022-01-31	Drug Facts
73057-378-11	2022-01-31	Drug Facts
73057-378-07	2022-01-28	Drug Facts
73057-378-08	2022-01-28	Drug Facts
73057-378-11	2022-01-28	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
73057-378-07	Senna-S	60 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	60	3
73057-378-08	Senna-S	100 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	100	3
73057-378-11	Senna-S	1000 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	1000	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73057-378	SENNA-S (SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG) TABLET, FILM COATED [ULAI HEALTH LLC]	3	Current NDC, Legacy NDC, 3 package rows	20250122_c0e27b02-8ef2-4239-8f8c-790f7d978dc0.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 12 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Well at Walgreens Castor Oil	CASTOR OIL	Walgreen Co.	e41f8553-3812-4d0b-95f8-20b261279299	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Walgreen Co.	b5a02809-6e01-4e01-b1c3-2b10c5091a4e	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Walgreen Co.	822fd02a-92b0-4010-8bfb-737dba331d54	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	Rugby Laboratories	5fd89979-903e-4b31-872d-3b8974af3a6b	2026-02-09	Warnings	Exact identifier application number: M007
Epsom Salt	EPSOM SALT	EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)	1845ea0c-0cb6-482b-abe6-fa17785c5b90	2026-02-09	Warnings	Exact identifier application number: M007
Colace Fast-Acting Saline Laxative	MAGNESIUM HYDROXIDE	Atlantis Consumer Healthcare, Inc.	572adfaf-6e26-42e5-b65d-6d356a0bdfa9	2026-02-06	Warnings	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Retail Business Services, LLC	4e9c41fa-f240-4986-bb13-541bfeb0e50b	2026-02-06	Warnings	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Retail Business Services, LLC	f3661952-ef4f-4f29-93e6-ec09b8464365	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Retail Business Services, LLC	2f6e9f87-4bff-482b-a54f-f51ca99aac8c	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Retail Business Services, LLC	1a8b540c-b66e-4dca-b7af-23705ae247b6	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Retail Business Services, LLC	b0abcdf9-c226-424f-8970-c2135708c6c8	2026-02-06	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Publix Super Markets, Inc.	e985e071-5541-456e-ae4d-dba85287fe75	2026-02-05	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Discount Drug Mart	a82a4aa9-c8af-4383-9d92-ba6c596f0095	2026-02-04	Warnings	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Discount Drug Mart	b05a94d2-5cc6-4989-9fb8-096e54fa7852	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Grocery Outlet, Inc.	3dff4b00-e71a-1dc0-e063-6394a90a715f	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	HARRIS TEETER	73065a04-b7cd-437d-9624-f845f5ec93bf	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M007
Harris Teeter	MINERAL	Harris Teeter	401e3a7e-54be-47cc-88c3-a343f5cbbd10	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Hy-Vee, Inc.	45374a86-80a4-481c-e063-6294a90a381a	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Hy-Vee, Inc.	44592ee0-13dd-57b1-e063-6394a90ab402	2026-02-04	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	CVS Pharmacy, Inc.	a78d991a-ba21-4bc4-b8f9-f8dafbddc28f	2026-02-03	Warnings, Adverse reactions	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	c0e27b02-8ef2-4239-8f8c-790f7d978dc0	3
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	c0e27b02-8ef2-4239-8f8c-790f7d978dc0	3
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	c0e27b02-8ef2-4239-8f8c-790f7d978dc0	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
73057-378-07	73057037807	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-378-07)	2019-07-10	0000-00-00	No	No	Current
73057-378-08	73057037808	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-378-08)	2019-07-10	0000-00-00	No	No	Current
73057-378-11	73057037811	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (73057-378-11)	2019-07-10	0000-00-00	No	No	Current