Senokot

Product NDC: 67618-120
11-digit product format: 676180120
Labeler code: 67618
Product ID: 67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da
Type: HUMAN OTC DRUG
Nonproprietary name: standardized senna concentrate
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Atlantis Consumer Healthcare, Inc.
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1988-09-01
Substance: SENNOSIDES
Active strength: 17.2 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	67618-120	67618-120-36	D	Discontinued by firm		2026-10-23

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 12 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

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	17.2 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
602802	Internal RxNorm lookup
1039965	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
d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
f52be47f-7aa7-46c0-b1fa-50c18dd50206	Product name	1	20201029

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
67618-120-06	Senokot	36 in 1 BOTTLE	TABLET, FILM COATED	36	11
67618-120-12	Senokot	12 in 1 BLISTER PACK	TABLET, FILM COATED	12	11
67618-120-12	Senokot	1 in 1 CARTON	TABLET, FILM COATED	1	11
67618-120-36	Senokot	12 in 1 BLISTER PACK	TABLET, FILM COATED	12	11
67618-120-36	Senokot	3 in 1 CELLO PACK	TABLET, FILM COATED	3	11
67618-120-72	Senokot	1 in 1 CARTON	TABLET, FILM COATED	1	11
67618-120-72	Senokot	2 in 1 PACKAGE	TABLET, FILM COATED	2	11
67618-120-73	Senokot	72 in 1 BOTTLE	TABLET, FILM COATED	72	11

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
67618-120-06	EA - Each	67618-120	77b005d4-d653-4a7e-8850-a12ceecdc616	1	2021-03-02
67618-120-12	EA - Each	67618-120	452e375b-566f-4df5-84ed-67a65d226ecc	1	2017-03-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67618-120	SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET, FILM COATED [ATLANTIS CONSUMER HEALTHCARE, INC.]	10	Current NDC, Legacy NDC, 8 package rows	20250419_d5bf67e5-82c6-edbf-e9ec-e027fdd47c84.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 31 of 42 · 829 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
HEB Stool Softener	DOCUSATE SODIUM	H E B	afc54b8e-03d9-418c-9322-97d68f929031	2024-12-18	Warnings	Exact identifier application number: M007
Foster and Thrive Gentle Laxative	BISACODYL	Strategic Sourcing Services LLC	d03c2c42-d9d9-4b4b-a6ae-31d99425a228	2024-12-18	Warnings	Exact identifier application number: M007
EX-LAX REGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE	SENNOSIDES	Haleon US Holdings LLC	59a26a7f-516f-4507-8dec-f40cf6cfaffc	2024-12-17	Warnings	Exact identifier application number: M007
EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE	SENNOSIDES	Haleon US Holdings LLC	fb170340-c996-46cf-b165-84e136ba4151	2024-12-17	Warnings	Exact identifier application number: M007
Senna Syrup	NATURAL VEGETABLE LAXATIVE	Bryant Ranch Prepack	7d1f092e-0e5b-4fed-a095-64449751582d	2024-12-16	Warnings	Exact identifier application number: M007
Drug Mart Vegetable Laxative plus Stool Softener	DOCUSATE SODIUM, SENNOSIDES	Discount Drug Mart, Inc	1b6d59e8-112f-447f-b6e9-526b7d3bd01e	2024-12-13	Warnings	Exact identifier application number: M007
Drug Mart Stool Softener plus Stimulant Laxative	DOCUSATE SODIUM, SENNOSIDES	Discount Drug Mart, Inc	caf74258-922c-4b69-9bd6-57b3e918c7a6	2024-12-13	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	National Vitamin Company	0c66642c-82cb-42cd-82bb-5f95852cc5d1	2024-12-12	Warnings	Exact identifier application number: M007
Foster and Thrive Fiber Laxative 147	CALCIUM POLYCARBOPHIL	Strategic Sourcing Services LLC	88d341a6-28aa-4a20-bfed-1d5f3106c2ae	2024-12-12	Warnings	Exact identifier application number: M007
Pedia-Lax	SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC	C.B. Fleet Company, Inc.	f001a37d-8ed4-428b-af12-d6a83c22c127	2024-12-12	Warnings	Exact identifier application number: M007
Careone Milk of magnesia Original Milk of Magnesia Original	MAGNESIUM HYDROXIDE	Retail Business Services, LLC.	13ffb00b-7c6f-47aa-bc82-2402d121a758	2024-12-11	Warnings	Exact identifier application number: M007
CareOne Milk of Magnesia Cherry	MAGNESIUM HYDROXIDE	Retail Business Services, LLC.	1822f90d-f693-48d7-b338-a3f2ddfac4df	2024-12-11	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	GOOD SENSE	a951b6d0-9182-e1bc-e053-2a95a90a12b1	2024-12-09	Warnings	Exact identifier application number: M007
milk of magnesia	MAGNESIUM HYDROXIDE	CVS Pharmacy	b3a36251-edd6-4201-8da1-85d7a6ede173	2024-12-05	Warnings	Exact identifier application number: M007
CITRUCEL	METHYLCELLULOSE	Haleon US Holdings LLC	d27f6742-2dcc-451e-b803-6ffe183038ec	2024-12-05	Warnings	Exact identifier application number: M007
Laxacin	DOCUSATE SODIUM AND SENNOSIDES	Alexso, Inc	0df9abaf-3997-4dde-8003-ae3d8d07cf39	2024-12-04	Warnings	Exact identifier application number: M007
NuValu Epsom Salt	MAGNESIUM SULFATE (HEPTAHYDRATE)	J C SALES	9f3cf9a4-e5c0-41ff-9fd3-63efb0d973cd	2024-12-04	Warnings	Exact identifier application number: M007
NuValu Epsom Salt	MAGNESIUM SULFATE (HEPTAHYDRATE)	J C SALES	5a503d8d-7899-4b1e-be6f-8e2a759af265	2024-12-04	Warnings	Exact identifier application number: M007
SENNOSIDES	SENNOSIDES	CVS Pharmacy, Inc.	6dffc3f5-bae0-c436-e053-2991aa0a0f8b	2024-12-02	Warnings	Exact identifier application number: M007
Pure and Gentle	MINERAL OIL	Medline Industries, LP	96d4cad5-0602-4c31-94ed-3117b4fd4a94	2024-11-26	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
602802	sennosides 17.2 MG Oral Tablet	PSN	d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	11
1039965	SenokotXTRA 17.2 MG Oral Tablet	PSN	d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	11
1039965	sennosides, USP 17.2 MG Oral Tablet [Senokot]	SBD	d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	11
602802	sennosides, USP 17.2 MG Oral Tablet	SCD	d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	11
1039965	Senokot 17.2 MG Oral Tablet	SY	d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	11
1039965	SenokotXTRA 17.2 MG Oral Tablet	SY	d5bf67e5-82c6-edbf-e9ec-e027fdd47c84	11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67618-120-06	67618012006	36 TABLET, FILM COATED in 1 BOTTLE (67618-120-06)		1988-09-01	0000-00-00	No	No	Current
67618-120-12	67618012012	1 BLISTER PACK in 1 CARTON (67618-120-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK	1 blister pack	1988-09-01	0000-00-00	No	No	Current
67618-120-36	67618012036	3 BLISTER PACK in 1 CELLO PACK (67618-120-36) > 12 BLISTER PACK in 1 BLISTER PACK > 12 TABLET, FILM COATED in 1 BLISTER PACK	3 blister pack	1988-09-01	2023-01-01	No	No	Current
67618-120-72	67618012072	2 CARTON in 1 PACKAGE (67618-120-72) / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE	2 carton	2024-01-01		No	No	Current
67618-120-73	67618012073	72 TABLET, FILM COATED in 1 BOTTLE (67618-120-73)		2025-11-15		No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
SenokotXTRA (standardizedsenna concentrate) Drug Facts	Atlantis Consumer Healthcare, Inc.	2025-08-20	HUMAN OTC DRUG LABEL	11