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 36 of 42 · 829 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stool Softener	DOCUSATE SODIUM	Sam's West, Inc	b14d2495-1092-4063-869f-73a7e8c28708	2024-05-21	Warnings	Exact identifier application number: M007
Stool Softener Plus Stimulant Laxative	DOCUSATE SODIUM AND SENNOSIDES	Safeway, Inc.	6bc9ea37-31b8-4a6d-9b2d-2c80bad4f30d	2024-05-15	Warnings	Exact identifier application number: M007
Stool Softener Plus Stimulant Laxative	DOCUSATE SODIUM AND SENNOSIDES	Safeway, Inc.	c0898583-4bbb-41d5-9e84-00cca823024f	2024-05-15	Warnings	Exact identifier application number: M007
Senna S	DOCUSATE SODIUM SENNOSIDES	QUALITY CHOICE (Chain Drug Marketing Association)	9c986ca8-d540-49c1-b092-94c1bf837c07	2024-05-09	Warnings	Exact identifier application number: M007
Fleet	GLYCERIN	C.B. Fleet Company, Inc.	381f4179-0c3b-41f8-927c-c88534ebe06d	2024-05-06	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	NuCare Pharmaceuticals,Inc.	ed20d198-e935-200e-e053-2a95a90a309b	2024-05-02	Warnings	Exact identifier application number: M007
Sennosides, Docusate Sodium	SENNOSIDES, DOCUSATE SODIUM	Major Pharmaceuticals	1768b470-2808-fa46-e063-6394a90ac8d9	2024-05-01	Warnings	Exact identifier application number: M007
Stool Softener Stimulant laxative	DOCUSATE SODIUM AND SENNOSIDES	QUALITY CHOICE (Chain Drug Marketing Association)	9467e1f7-19bb-4fb3-853b-75c4d28bb9a9	2024-05-01	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM AND SENNOSIDES	QUALITY CHOICE (Chain Drug Marketing Association)	72f8e8d7-ee38-4bd3-8711-f11fded0cede	2024-05-01	Warnings	Exact identifier application number: M007
Stool Softener Laxative Extra Strength	DOCUSATE SODIUM	P & L Development, LLC	c1e9863a-c229-4694-b450-6b0e0ad37503	2024-04-30	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	QUALITY CHOICE (Chain Drug Marketing Association)	96c7f8bc-be95-40d1-9977-44b7cc6582df	2024-04-22	Warnings	Exact identifier application number: M007
Pedia-Lax	MAGNESIUM HYDROXIDE	C.B. Fleet Company, Inc.	975f24d8-218c-40f4-84a5-558acf34329d	2024-04-11	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM AND SENNOSIDES	H E B	2f9e2723-53a7-47a8-8c41-87bffc4e50dd	2024-04-09	Warnings	Exact identifier application number: M007
Senna	SENNOSIDES	H E B	d047e4e9-b8ac-498e-9fde-8af5d415edaa	2024-04-09	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	H E B	5b8bcc6c-de03-4d73-a76f-6f4c371cf250	2024-04-09	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	H E B	1dd2be7e-bdca-4e43-b853-3ed10b636632	2024-04-08	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	Bryant Ranch Prepack	1f11cf85-b094-4ca4-8b48-2d3a9093304b	2024-04-04	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	TARGET Corporation	89106733-69f1-469b-9d07-f06ac09b2fb6	2024-04-02	Warnings	Exact identifier application number: M007
Stool Softener Laxative Plus Stimulant	DOCUSATE SODIUM AND SENNOSIDES	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	89dc2063-6744-4412-89be-90990090b57c	2024-03-19	Warnings	Exact identifier application number: M007
Senna Laxative	SENNOSIDES	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	2322765d-6f08-48d4-a500-818a8a558f6f	2024-03-19	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