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 11 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mineral Oil	MINERAL OIL	United Natural Foods, Inc. dba UNFI	cb7bc571-295f-47c2-ae93-18cba194752c	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Strategic Sourcing Services LLC	e4965086-dcc0-4b34-bb30-81facf7139f3	2026-02-17	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Valu Merchandisers Company	cd3e5836-b2f0-41f3-8623-3105c4642491	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGESIUM CITRATE	Valu Merchandisers Company	a693f6b0-0679-4609-9ca0-dddfa4158c02	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Valu Merchandisers Company	fb358bc3-e479-42e7-8aea-a6a3676f2430	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Valu Merchandisers Company	ff539c1c-9ed3-49be-9b30-1858f12e1e90	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
Castor Oil	CASTOR OIL	United Natural Foods, Inc. dba UNFI	bd19bea3-5ac9-4f8d-b1a0-478fd9c8a01f	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
Walgreens SmoothLAX Soft Chews	MAGNESIUM HYDROXIDE	Walgreens	424e27ce-0b11-9cd2-e063-6294a90a3c21	2026-02-16	Warnings	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	United Natural Foods, Inc. dba UNFI	da013c15-3531-4dc5-b122-bfc99bc494ae	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	United Natural Foods, Inc. dba UNFI	db1bc651-1a35-4f92-a917-c6a19f421594	2026-02-16	Warnings, Adverse reactions	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	The Kroger Co.	e1a68bd9-d31a-46a6-8c08-7ad8197b6e0b	2026-02-13	Warnings	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Topco Associates LLC	b2ec06b3-647d-49ab-a392-6db63d96d1e3	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Topco Associates LLC	5643f2e0-93e2-4c2e-90a0-fd152150d18a	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGESIUM CITRATE	Topco Associates LLC	d3cc7cb6-098e-413c-b1ad-7ebf5fa35269	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M007
citroma	MAGNESIUM CITRATE	Topco Associates LLC	bc89c4bc-5207-479d-9a3b-e570b412a7ba	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Topco Associates LLC	72f69aa0-381a-4e5c-975d-3a73fdc1b377	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Topco Associates LLC	e9b1fd61-c229-4529-82c2-d6ac5b076082	2026-02-13	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Pinnacle RX LLC	4abbb0e4-e005-bc4e-e063-6394a90a126a	2026-02-13	Warnings, Adverse reactions	Exact identifier application number: M007
365 Whole Foods Market Epsom Salt	MAGNESIUM SULFATE	Whole Foods Market, Inc.	4147cdd0-57f6-3857-e063-6394a90afecb	2026-02-12	Warnings, Adverse reactions	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Your Military Exchanges	27cff497-123c-424a-9c43-57740c00168b	2026-02-12	Warnings, Adverse reactions	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