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 7 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sennosides, Docusate Sodium	SENNOSIDES, DOCUSATE SODIUM	Cardinal Health 107, LLC	1a21b07a-263c-41a4-ba0c-ad2dc5a295d7	2026-05-05	Warnings	Exact identifier application number: M007
Docusate Sodium and Sennosides	DOCUSATE SODIUM AND SENNOSIDES	SOFTGEL HEALTHCARE PRIVATE LIMITED	4842a767-bb12-9d85-e063-6294a90a19b5	2026-04-27	Warnings	Exact identifier application number: M007
Alcohol wet wipes	ALCOHOL WET WIPES	Shandong Aishule Hygiene Products Co., Ltd	f79dbac0-cec0-46bc-e053-6294a90a2b13	2026-04-25	Warnings	Exact identifier application number: M007
Sterilized wet wipes	STERILIZED WET WIPES	Shandong Aishule Hygiene Products Co., Ltd	f7ca1799-eee4-66f0-e053-6294a90a273f	2026-04-25	Warnings	Exact identifier application number: M007
Wet wipes	WET WIPES	JINGXIN GROUP (M) SDN BHD	395225b1-486b-1867-e063-6394a90a1865	2026-04-25	Warnings	Exact identifier application number: M007
Sterilized wet wipes	STERILIZED WET WIPES	JINGXIN GROUP (M) SDN BHD	3952873e-5e3f-1bff-e063-6294a90a8a62	2026-04-25	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Publix Supermarkets, Inc.	ed50555f-b105-45c8-9dc4-1bd4d233a1e3	2026-04-23	Warnings	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Publix Supermarkets, Inc.	382a57d1-85bf-480f-9967-f85da2904410	2026-04-23	Warnings	Exact identifier application number: M007
BISACODYL	BISACODYL	AARNA USA INC.	50109967-69af-5fc5-e063-6394a90a8751	2026-04-22	Warnings	Exact identifier application number: M007
Senna	SENNA	Rugby Laboratories	41d53783-7ac2-411c-b9bf-afd87b3af30d	2026-04-18	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	United Natural Foods, Inc. dba UNFI	95bae7bf-f240-4674-9e3c-640a603fdc35	2026-04-15	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Publix Super Markets, Inc.	a4b442f1-d5a6-4cbf-b371-1f6639634f80	2026-04-13	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Publix Super Markets, Inc.	267c434d-3034-491b-b4b1-1d0cbacb1615	2026-04-13	Warnings, Adverse reactions	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Bryant Ranch Prepack	d616685a-11fc-4ae0-80de-7d25c0d71ee9	2026-04-09	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	H E B	84116db2-a7b7-460a-a5e5-8558bd424781	2026-04-02	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA ORIGINAL	MAGNESIUM HYDROXIDE	American Health Packaging	7d7d789b-b2e7-4600-a025-0cd2ff5b3672	2026-04-02	Warnings	Exact identifier application number: M007
Castor Oil	CASTOR OIL	STRATEGIC SOURCING SERVICES	4db6736f-416a-f142-e063-6394a90ab08f	2026-04-01	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Farmacias De Similares TX LLC	4e6a64a0-e453-709b-e063-6294a90a7443	2026-04-01	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Major Pharmaceuticals	93ef6486-0930-41e3-a2c6-44af7e37e98b	2026-03-31	Warnings	Exact identifier application number: M007
Senna Syrup	NATURAL VEGETABLE LAXATIVE	Bryant Ranch Prepack	2c0d62e7-563b-46e4-9793-183e98e761a6	2026-03-25	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