Senokot-S

Product NDC: 67618-310
11-digit product format: 676180310
Labeler code: 67618
Product ID: 67618-310_e5dc8b86-705c-4b54-a9fe-20d02d62ad48
Type: HUMAN OTC DRUG
Nonproprietary name: standardized senna concentrate and docusate sodium
Dosage form: TABLET
Route: ORAL
Labeler: Atlantis Consumer Healthcare, Inc.
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1974-10-01
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

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-S
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 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
998740	Internal RxNorm lookup
1248015	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
c24cdc5e-62e0-41a6-8afb-512202a569f4	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
67618-310-01	Senokot-S	1 in 1 CARTON	TABLET	1	11
67618-310-01	Senokot-S	10 in 1 BLISTER PACK	TABLET	10	11
67618-310-30	Senokot-S	1 in 1 CARTON	TABLET	1	11
67618-310-30	Senokot-S	30 in 1 BOTTLE, PLASTIC	TABLET	30	11
67618-310-60	Senokot-S	60 in 1 BOTTLE, PLASTIC	TABLET	60	11
67618-310-60	Senokot-S	1 in 1 CARTON	TABLET	1	11

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
67618-310-01	EA - Each	67618-310	fca641d4-5032-4c8a-89b0-1531d188c82e	1	2012-07-24
67618-310-11	EA - Each	67618-310	b217ce91-d971-47fa-b151-c25b031e0673	1	2012-07-24
67618-310-30	EA - Each	67618-310	92a84d0c-0e14-4556-be2d-d25805cb714f	1	2012-07-24
67618-310-60	EA - Each	67618-310	d8f7c560-0b44-4674-9a72-8d1dece16702	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DOCUSATE SODIUM	ACTIVE INGREDIENT	F05Q2T2JA0	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
SENNOSIDES	ACTIVE INGREDIENT	3FYP5M0IJX	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
DOCUSATE	ACTIVE MOIETY	M7P27195AG	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
SENNOSIDES	ACTIVE MOIETY	3FYP5M0IJX	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
EGG PHOSPHOLIPIDS	INACTIVE INGREDIENT	1Z74184RGV	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
POLYVINYL ALCOHOL	INACTIVE INGREDIENT	532B59J990	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
SODIUM BENZOATE	INACTIVE INGREDIENT	OJ245FE5EU	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [PURDUE PRODUCTS LP]	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67618-310	SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [ATLANTIS CONSUMER HEALTHCARE, INC.]	10	Current NDC, Legacy NDC, 6 package rows	20241228_c24cdc5e-62e0-41a6-8afb-512202a569f4.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	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
1248015	Senokot-S 8.6 MG / 50 MG Oral Tablet	PSN	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
1248015	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [SENOKOT-S]	SBD	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
998740	docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SCD	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
998740	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet	SY	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
1248015	DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [SENOKOT-S]	SY	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
1248015	SENOKOT-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral Tablet	SY	c24cdc5e-62e0-41a6-8afb-512202a569f4	11
1248015	SENOKOT-S Oral Tablet	SY	c24cdc5e-62e0-41a6-8afb-512202a569f4	11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67618-310-01	67618031001	1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK	1 blister pack	1974-10-01	0000-00-00	No	No	Current
67618-310-10	67618031010	1 BOTTLE, PLASTIC in 1 CARTON (67618-310-10) / 100 TABLET in 1 BOTTLE, PLASTIC		2026-09-30		No	No	Current
67618-310-30	67618031030	1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC		1974-10-01	0000-00-00	No	No	Current
67618-310-60	67618031060	1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC		1974-10-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Senokot-S (standardizedsenna concentrate and docusate sodium)	Atlantis Consumer Healthcare, Inc.	2026-08-21	HUMAN OTC DRUG LABEL	12