Sankaijo

Product NDC: 49873-404
11-digit product format: 498730404
Labeler code: 49873
Product ID: 49873-404_0b54b2d1-83e7-3a18-e063-6394a90a5b58
Type: HUMAN OTC DRUG
Nonproprietary name: docusate sodium, sennosides
Dosage form: TABLET
Route: ORAL
Labeler: Sato Pharmaceutical Co., Ltd.
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2002-12-20
Substance: DOCUSATE SODIUM; SENNOSIDES
Active strength: 8.33; 1.36 mg/1; mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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 · 4 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2019-12-08 06:16 UTC · source 2019-12-05	unfinished product	product		`263afe128892…`	`91768de4ddbe…`
2019-12-08 06:16 UTC · source 2019-12-05	unfinished package	package	49873-404-90	`263afe128892…`	`91768de4ddbe…`
2019-06-01 22:24 UTC · source 2019-05-30	unfinished product	product		`5b2001dcd8f5…`	`54b53d4dc9e4…`
2019-06-01 22:24 UTC · source 2019-05-30	unfinished package	package	49873-404-90	`5b2001dcd8f5…`	`54b53d4dc9e4…`

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: Sankaijo
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DOCUSATE SODIUM	8.33 mg/1
SENNOSIDES	1.36 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
F05Q2T2JA0	Internal UNII lookup
3FYP5M0IJX	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1235252	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
83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49873-404-01	Sankaijo	1 in 1 CARTON	TABLET	1		11
49873-404-01	Sankaijo	150 in 1 BOTTLE	TABLET	150		11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
docusate sodium	ACTIVE INGREDIENT	F05Q2T2JA0	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
SENNOSIDES	ACTIVE INGREDIENT	3FYP5M0IJX	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
docusate	ACTIVE MOIETY	M7P27195AG	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
SENNOSIDES	ACTIVE MOIETY	3FYP5M0IJX	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS	INACTIVE INGREDIENT	L11K75P92J	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
caramel	INACTIVE INGREDIENT	T9D99G2B1R	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
CARBOXYMETHYLCELLULOSE CALCIUM	INACTIVE INGREDIENT	UTY7PDF93L	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
DIMETHICONE	INACTIVE INGREDIENT	92RU3N3Y1O	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
FENNEL	INACTIVE INGREDIENT	557II4LLC3	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
HYPROMELLOSE 2910 (15000 MPA.S)	INACTIVE INGREDIENT	288VBX44JC	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
IPOMOEA NIL SEED	INACTIVE INGREDIENT	I85W45B4WB	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
PAEONIA SUFFRUTICOSA ROOT BARK	INACTIVE INGREDIENT	BUG255FE7X	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
PEG/PPG-105/5 COPOLYMER	INACTIVE INGREDIENT	52901V8XAR	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49873-404	SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]	11	Current NDC, Legacy NDC, 2 package rows	20231130_83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b.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 8 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Laxomil	BISACODYL 5MG	Pharmadel LLC	3999935b-d8e8-52a6-e063-6294a90aa2a2	2026-03-20	Warnings	Exact identifier application number: M007
Laxative Enteric Coated	BISACODYL 5MG	Grocery Outlet	c820e6a1-fa23-447a-9ee9-50a1bd617adb	2026-03-19	Warnings	Exact identifier application number: M007
CITRUCEL	METHYLCELLULOSE	Haleon US Holdings LLC	9d5f2244-a610-4d45-b6e8-e79bb17a558f	2026-03-18	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Safeway, Inc.	f178b31d-4843-4b91-a0d5-ab5ade835dc2	2026-03-16	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Safeway, Inc.	12ab9c3c-1f4b-43cd-83ac-b5f80b1aa54c	2026-03-13	Warnings	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Old East Main Co.	a1ca668a-3bf9-46a9-8a4f-5cb61547bb81	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Vi-Jon, LLC	b29775df-8470-4fe3-bee3-f0490ea6903f	2026-03-12	Warnings	Exact identifier application number: M007
Castor Oil	CASTOR OIL	Nice-Pak Products, LLC	cc43d514-ee82-4314-99b2-c64380f98779	2026-03-12	Warnings, Adverse reactions	Exact identifier application number: M007
Fibercon	CALCIUM POLYCARBOPHIL	Foundation Consumer Brands	7992a4bb-5535-4a1d-867d-a99f7e0c1be7	2026-03-12	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Walgreens	cda27a9c-9175-4b07-9c0b-d8d897882965	2026-03-12	Warnings	Exact identifier application number: M007
Magnesium Citrate Saline Laxative - Lemon Flavor	MAGNESIUM CITRATE	Universal Distribution Center LLC	aa02c9af-22b8-4ec2-9e43-fe073f5e617b	2026-03-11	Warnings	Exact identifier application number: M007
Magnesium Citrate Saline Laxative - Grape Flavor	MAGNESIUM CITRATE	Universal Distribution Center LLC	021ebb61-2466-4272-8f7d-b49cafd08754	2026-03-11	Warnings	Exact identifier application number: M007
Magnesium Citrate Saline Laxative - Cherry Flavor	MAGNESIUM CITRATE	Universal Distribution Center LLC	1f14411b-6833-40e6-b1a5-2b8c5bf709d3	2026-03-11	Warnings	Exact identifier application number: M007
Citroma	MAGNESIUM CITRATE	UpLift Brands, LLC	f83ba007-734d-4910-87cb-02e45285e161	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M007
Citroma	MAGNESIUM CITRATE	UpLift Brands, LLC	57e914fa-8fa2-4221-bb5f-534f0ea0aba7	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M007
Citroma	MAGNESIUM CITRATE	UpLift Brands, LLC	f28a9043-e0ee-4b38-95d9-d3f23d400691	2026-03-11	Warnings, Adverse reactions	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	Amerisource Bergen	4caf0bcb-c1bf-0ae7-e063-6294a90a344b	2026-03-10	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Walgreens	92df761b-da68-4ce9-b02a-a5a74fd6620e	2026-03-10	Warnings	Exact identifier application number: M007
Fleet	GLYCERIN	C.B. Fleet Company, Inc.	31778652-e60e-4098-8e90-3e4f56b5800c	2026-03-06	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN	Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd	4c6094b7-c1ef-26a3-e063-6394a90af4cc	2026-03-06	Warnings	Exact identifier application number: M007

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F05Q2T2JA0	DOCUSATE SODIUM	577-11-7	DOCUSATE SODIUM
3FYP5M0IJX	SENNOSIDES		SENNOSIDES

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1235252	docusate sodium 8.33 MG / sennosides 1.36 MG Oral Tablet	PSN	83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b	11
1235252	docusate sodium 8.33 MG / sennosides, USP 1.36 MG Oral Tablet	SCD	83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b	11
1235252	DOSS Sodium 8.33 MG / sennosides, USP 1.36 MG Oral Tablet	SY	83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b	11

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
49873-404-01	49873040401	1 BOTTLE in 1 CARTON (49873-404-01) / 150 TABLET in 1 BOTTLE	1 bottle	2002-12-20	0000-00-00	No	No	Current