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 40 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Milk of Magnesia mint	MAGNESIUM HYDROXIDE	Meijer, Inc.	bb8ba371-f53c-1088-e053-2a95a90a4cbf	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	STRATEGIC SOURCING SERVICES LLC	00c61622-367b-0a5b-e063-6294a90a6706	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Strategic Sourcing Services LLC	003a3c0d-7a48-e44d-e063-6394a90a3f4a	2023-11-08	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	Geri-Care Pharmaceuticals, Corp	2d1be236-e136-4727-a52d-714f62880088	2023-11-08	Warnings	Exact identifier application number: M007
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

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