Senokot

Product NDC: 67618-300
11-digit product format: 676180300
Labeler code: 67618
Product ID: 67618-300_fd1324ab-ef79-42ee-b960-9b032a3a4af2
Type: HUMAN OTC DRUG
Nonproprietary name: standardized senna concentrate
Dosage form: TABLET
Route: ORAL
Labeler: Atlantis Consumer Healthcare, Inc.
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1956-06-01
Substance: SENNOSIDES
Active strength: 8.6 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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: Senokot
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SENNOSIDES	8.6 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
312935	Internal RxNorm lookup
404186	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
c18dd7fa-993b-440b-8cdd-f1551abb99ca	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
67618-300-10	Senokot	1 in 1 CARTON	TABLET	1	12
67618-300-10	Senokot	100 in 1 BOTTLE, PLASTIC	TABLET	100	12
67618-300-20	Senokot	10 in 1 BLISTER PACK	TABLET	10	12
67618-300-20	Senokot	2 in 1 CARTON	TABLET	2	12
67618-300-50	Senokot	1 in 1 CARTON	TABLET	1	12
67618-300-50	Senokot	50 in 1 BOTTLE, PLASTIC	TABLET	50	12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
67618-300-10	EA - Each	67618-300	6d995b3f-8f49-4111-9050-f18f3f0be499	1	2012-07-24
67618-300-11	EA - Each	67618-300	550247ea-a7f8-4d6f-9cd9-b442d2c9f6d1	1	2012-07-24
67618-300-20	EA - Each	67618-300	029befb9-b71d-41e1-8118-4fac1a66fc44	1	2012-07-24
67618-300-40	EA - Each	67618-300	147e5b3d-423c-45e9-8222-6f15b35fc06d	1	2013-06-04
67618-300-50	EA - Each	67618-300	e8768eff-fab6-4153-9fa7-44686f5e8f05	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
SENNOSIDES	ACTIVE INGREDIENT	3FYP5M0IJX	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]	3
SENNOSIDES	ACTIVE MOIETY	3FYP5M0IJX	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]	3
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]	3
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67618-300	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [ATLANTIS CONSUMER HEALTHCARE, INC.]	11	Current NDC, Legacy NDC, 6 package rows	20241228_c18dd7fa-993b-440b-8cdd-f1551abb99ca.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 · 829 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
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
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Wal-Mart Stores, Inc.	750e0355-369e-b679-e053-2a91aa0a66ca	2023-11-01	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Wal-Mart Stores, Inc.	750efd58-5845-fbc4-e053-2a91aa0a86d1	2023-11-01	Warnings	Exact identifier application number: M007
Gentle Laxative	MAGNESIUM HYDROXIDE	WALGREEN COMPANY	ba4a29b3-2ddc-b906-e053-2995a90a2ab7	2023-11-01	Warnings	Exact identifier application number: M007
DOCUZEN	SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG	Proficient Rx LP	92879e62-f60a-4ab4-9532-610cdd2628ee	2023-11-01	Warnings	Exact identifier application number: M007

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
3FYP5M0IJX	SENNOSIDES	SENNOSIDES

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312935	sennosides 8.6 MG Oral Tablet	PSN	c18dd7fa-993b-440b-8cdd-f1551abb99ca	12
404186	Senokot 8.6 MG Oral Tablet	PSN	c18dd7fa-993b-440b-8cdd-f1551abb99ca	12
404186	sennosides, USP 8.6 MG Oral Tablet [Senokot]	SBD	c18dd7fa-993b-440b-8cdd-f1551abb99ca	12
312935	sennosides, USP 8.6 MG Oral Tablet	SCD	c18dd7fa-993b-440b-8cdd-f1551abb99ca	12
312935	sennosides A and B 8.6 MG Oral Tablet	SY	c18dd7fa-993b-440b-8cdd-f1551abb99ca	12
404186	Senokot 8.6 MG Oral Tablet	SY	c18dd7fa-993b-440b-8cdd-f1551abb99ca	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67618-300-10	67618030010	1 BOTTLE, PLASTIC in 1 CARTON (67618-300-10) / 100 TABLET in 1 BOTTLE, PLASTIC		1956-06-01	0000-00-00	No	No	Current
67618-300-20	67618030020	2 BLISTER PACK in 1 CARTON (67618-300-20) / 10 TABLET in 1 BLISTER PACK	2 blister pack	1956-06-01	0000-00-00	No	No	Current
67618-300-50	67618030050	1 BOTTLE, PLASTIC in 1 CARTON (67618-300-50) / 50 TABLET in 1 BOTTLE, PLASTIC		1956-06-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SENOKOT	A-S Medication Solutions	2026-09-09	HUMAN OTC DRUG LABEL	1
Senokot (standardized senna concentrate)	Atlantis Consumer Healthcare, Inc.	2025-12-29	HUMAN OTC DRUG LABEL	12