Stool Softener Laxative

Product NDC: 0904-7280
11-digit product format: 009047280
Labeler code: 0904
Product ID: 0904-7280_9106599b-ff0f-4d97-a4e4-ce9ca098e23c
Type: HUMAN OTC DRUG
Nonproprietary name: DOCUSATE SODIUM
Dosage form: CAPSULE, LIQUID FILLED
Route: ORAL
Labeler: Major Pharmaceuticals
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2022-11-15
Substance: DOCUSATE SODIUM
Active strength: 100 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Stool Softener Laxative
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DOCUSATE SODIUM	100 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

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

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1115005	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
97561cd4-63d9-44c2-a3a3-ec668a09a4ed	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6084a4f4-5437-c9a5-caec-5361ee075a59	Product name	1	20140508
90c5639a-61b0-88d6-ddcf-21888e94869a	Product name	1	20140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0904-7280-60	Stool Softener Laxative	100 in 1 BOTTLE, PLASTIC	CAPSULE, LIQUID FILLED	100		9
0904-7280-80	Stool Softener Laxative	1000 in 1 BOTTLE, PLASTIC	CAPSULE, LIQUID FILLED	1000		9

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0904-7280-60	EA - Each	0904-7280	26a1e584-5c99-4037-9a6b-ca3b57d707f2	1	2023-03-13
0904-7280-80	EA - Each	0904-7280	d88438cf-e71a-4f39-b013-ee79652343c4	1	2023-03-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0904-7280	STOOL SOFTENER LAXATIVE (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MAJOR PHARMACEUTICALS]	8	Current NDC, Legacy NDC, 2 package rows	20240904_97561cd4-63d9-44c2-a3a3-ec668a09a4ed.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 1 of 44 · 878 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SENOKOT	STANDARDIZED SENNA	A-S Medication Solutions	0c6e6bdd-9f49-4550-b60a-8f58b7c0f090	2026-09-09	Warnings	Exact identifier application number: M007
Bisacodyl	BISACODYL	KROGER COMPANY	a13a8eec-3652-8c57-e053-2995a90aaebf	2026-09-09	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	TARGET Corporation	4180a35b-cc50-46ae-a100-99bb218c10ff	2026-09-09	Warnings	Exact identifier application number: M007
fiber laxative	PSYLLIUM HUSK	Raritan Pharmaceuticals Inc	22e927bd-5734-424e-8870-1aaa18f1265e	2026-09-08	Warnings	Exact identifier application number: M007
DRx Choice Fiber Therapy	METHYLCELLULOSE	RARITAN PHARMACEUTICALS INC	5e5749f7-074e-4bbc-9f33-5090e603fdb4	2026-09-08	Warnings	Exact identifier application number: M007
Bisacodyl Stimulant Laxative	BISACODYL	Raritan Pharmaceuticals Inc	b99c1a6d-3034-4822-8540-210179c06857	2026-09-08	Warnings	Exact identifier application number: M007
Daily Fiber Sugar Free	PSYLLIUM HUSK	Raritan Pharmaceuticals Inc	9c4c41d8-a2d5-4168-9e97-9f9d47fc5e63	2026-09-08	Warnings	Exact identifier application number: M007
DRx Choice Fiber Therapy	METHYLCELLULOSE	RARITAN PHARMACEUTICALS INC	56c7f197-f01a-4611-a761-cda18da6eed0	2026-09-08	Warnings	Exact identifier application number: M007
Sennosides 8.6 mg	SENNOSIDES	Morepen Bio Inc	562c9f11-0ba1-011d-e063-6394a90a604a	2026-09-05	Warnings	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Target Corporation	87f98e6c-a3a1-4ca5-bd56-977e38f48914	2026-09-04	Warnings, Adverse reactions	Exact identifier application number: M007
Kroger Stool Softener Fruit Punch	DOCUSATE SODIUM	KROGER COMPANY	b86f8f3d-594e-466c-854a-b8bff9f7a0b8	2026-09-02	Warnings	Exact identifier application number: M007
Oil	MINERAL OIL	Atlantic Biologicals Corp.	5a82197b-281d-76c0-e063-6294a90a5746	2026-09-02	Warnings, Adverse reactions	Exact identifier application number: M007
Kroger Senna Laxative Regular Strength	SENNOSIDES	KROGER COMPANY	dbb040bb-21f9-43e8-9705-689aeee4d04c	2026-09-01	Warnings	Exact identifier application number: M007
OneLAX SENNA	SENNA	Akron Pharma Inc.	27fa8f54-ed84-4afd-8da3-8754da48643b	2026-09-01	Warnings	Exact identifier application number: M007
OneLAX Saline Laxative	MAGNESIUM CITRATE	AKRON PHARMA INC	44c87bbc-2507-4b87-a74b-02f4acb30cf4	2026-09-01	Warnings	Exact identifier application number: M007
OneLAX Saline Laxative	MAGNESIUM CITRATE	AKRON PHARMA INC	e6de00e6-dd81-4aab-af23-04fab261c6ff	2026-09-01	Warnings	Exact identifier application number: M007
EZ2Go Magnesium Citrate Saline Laxative Lemon Flavor	MAGNESIUM CITRATE	Valley Medical Products LLC	5a71e88c-d8cc-a8bb-e063-6294a90af4f7	2026-09-01	Warnings	Exact identifier application number: M007
Fiber Caplets	CALCIUM POLYCARBOPHIL	THE KROGER CO.	d6856f59-ccc3-40fc-9bf1-7a5394ed12da	2026-09-01	Warnings	Exact identifier application number: M007
Mineral Oil	MINERAL OIL	Your Military Exchanges	6025dce6-02e8-418c-a248-0b5c33ff6067	2026-08-28	Warnings, Adverse reactions	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Chain Drug Marketing Association	583b64e7-e48d-6ba6-e063-6294a90ad4d7	2026-08-28	Warnings, Adverse reactions	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1115005	docusate sodium 100 MG Oral Capsule	PSN	d616685a-11fc-4ae0-80de-7d25c0d71ee9	104
1115005	docusate sodium 100 MG Oral Capsule	SCD	d616685a-11fc-4ae0-80de-7d25c0d71ee9	104
1115005	DOSS Sodium 100 MG Oral Capsule	SY	d616685a-11fc-4ae0-80de-7d25c0d71ee9	104
1115005	docusate sodium 100 MG Oral Capsule	PSN	5d300ea7-78eb-4e19-8333-1e42c73c4c54	10
1115005	docusate sodium 100 MG Oral Capsule	SCD	5d300ea7-78eb-4e19-8333-1e42c73c4c54	10
1115005	DOSS Sodium 100 MG Oral Capsule	SY	5d300ea7-78eb-4e19-8333-1e42c73c4c54	10
1115005	docusate sodium 100 MG Oral Capsule	PSN	97561cd4-63d9-44c2-a3a3-ec668a09a4ed	9
1115005	docusate sodium 100 MG Oral Capsule	SCD	97561cd4-63d9-44c2-a3a3-ec668a09a4ed	9
1115005	DOSS Sodium 100 MG Oral Capsule	SY	97561cd4-63d9-44c2-a3a3-ec668a09a4ed	9
1115005	docusate sodium 100 MG Oral Capsule	PSN	867a7771-6846-427d-b526-b964d74f7700	4
1115005	docusate sodium 100 MG Oral Capsule	SCD	867a7771-6846-427d-b526-b964d74f7700	4
1115005	DOSS Sodium 100 MG Oral Capsule	SY	867a7771-6846-427d-b526-b964d74f7700	4
1115005	docusate sodium 100 MG Oral Capsule	PSN	4d678da0-9ada-4d00-9db9-33b45c776107	3
1115005	docusate sodium 100 MG Oral Capsule	SCD	4d678da0-9ada-4d00-9db9-33b45c776107	3
1115005	DOSS Sodium 100 MG Oral Capsule	SY	4d678da0-9ada-4d00-9db9-33b45c776107	3
1115005	docusate sodium 100 MG Oral Capsule	PSN	ccfa095c-77f0-41ff-84f8-e02d983c7c74	2
1115005	docusate sodium 100 MG Oral Capsule	PSN	fdf3c8e1-d554-4cdb-e053-6394a90a542e	2
1115005	docusate sodium 100 MG Oral Capsule	SCD	ccfa095c-77f0-41ff-84f8-e02d983c7c74	2
1115005	docusate sodium 100 MG Oral Capsule	SCD	fdf3c8e1-d554-4cdb-e053-6394a90a542e	2
1115005	DOSS Sodium 100 MG Oral Capsule	SY	fdf3c8e1-d554-4cdb-e053-6394a90a542e	2
1115005	DOSS Sodium 100 MG Oral Capsule	SY	ccfa095c-77f0-41ff-84f8-e02d983c7c74	2
1115005	docusate sodium 100 MG Oral Capsule	PSN	2c65319f-6cf5-aa90-e063-6394a90ad662	1
1115005	docusate sodium 100 MG Oral Capsule	SCD	2c65319f-6cf5-aa90-e063-6394a90ad662	1
1115005	DOSS Sodium 100 MG Oral Capsule	SY	2c65319f-6cf5-aa90-e063-6394a90ad662	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0904-7280-60	00904728060	100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0904-7280-60)	2022-11-15	0000-00-00	No	No	Current
0904-7280-80	00904728080	1000 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0904-7280-80)	2022-11-15	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
DRUG FACTS	Bryant Ranch Prepack	2026-04-09	HUMAN OTC DRUG LABEL	104
DRUG FACTS	Preferred Pharmaceuticals Inc.	2026-04-08	HUMAN OTC DRUG LABEL	4
DRUG FACTS	PD-Rx Pharmaceuticals, Inc.	2026-02-26	HUMAN OTC DRUG LABEL	10
DRUG FACTS	Major Pharmaceuticals	2025-10-31	HUMAN OTC DRUG LABEL	9
DRUG FACTS	NuCare Pharmaceuticals, Inc.	2025-01-23	HUMAN OTC DRUG LABEL	1
DRUG FACTS	NCS HealthCare of KY, LLC dba Vangard Labs	2025-01-15	HUMAN OTC DRUG LABEL	3
DRUG FACTS	NuCare Pharmaceuticals,Inc.	2024-11-01	HUMAN OTC DRUG LABEL	2
DRUG FACTS	Proficient Rx LP	2024-08-01	HUMAN OTC DRUG LABEL	2