good sense stool softener

Product NDC: 0113-0486
11-digit product format: 001130486
Labeler code: 0113
Product ID: 0113-0486_1fcced0d-ec08-467a-8918-73d8df989fd1
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate sodium
Dosage form: CAPSULE, LIQUID FILLED
Route: ORAL
Labeler: L. Perrigo Company
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1991-10-29
Substance: DOCUSATE SODIUM
Active strength: 100 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	0113-0486	0113-0486-72	D	Discontinued by firm		2026-10-15

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 · 23 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
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0113-0486-72	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0113-0486-72	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0113-0486-72	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0113-0486-72	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0113-0486-72	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0113-0486-72	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0113-0486-72	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0113-0486-72	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0113-0486-72	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0113-0486-72	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0113-0486-72	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0113-0486-72	`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: good sense stool softener
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
4658d162-6e62-4d84-b5d6-7bf16c915558	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0113-0486-72	good sense stool softener	1 in 1 CARTON	CAPSULE, LIQUID FILLED	1	5
0113-0486-72	good sense stool softener	60 in 1 BOTTLE	CAPSULE, LIQUID FILLED	60	5
0113-0486-78	good sense stool softener	100 in 1 BOTTLE	CAPSULE, LIQUID FILLED	100	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0113-0486-72	EA - Each	0113-0486	a941655f-c07b-43a1-a078-48c78c3d4cea	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DOCUSATE SODIUM	ACTIVE INGREDIENT	F05Q2T2JA0	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
DOCUSATE	ACTIVE MOIETY	M7P27195AG	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
D&C RED NO. 33	INACTIVE INGREDIENT	9DBA0SBB0L	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
GELATIN	INACTIVE INGREDIENT	2G86QN327L	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
SORBITAN	INACTIVE INGREDIENT	6O92ICV9RU	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
SORBITOL	INACTIVE INGREDIENT	506T60A25R	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	GOOD SENSE STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [L PERRIGO COMPANY]	1

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 20 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
up and up fiber therapy	PSYLLIUM HUSK	Target Corporation	674753ee-1174-4c06-9ed3-a090b338a39e	2025-11-05	Warnings	Exact identifier application number: M007
up and up fiber therapy	PSYLLIUM HUSK	TARGET CORPORATION	956c48f8-c705-4a86-9866-c68a48ddeb6c	2025-11-05	Warnings	Exact identifier application number: M007
CEO-TWO	LAXATIVE	Beutlich Pharmaceuticals, LLC	08670636-5795-4db0-e063-6294a90afa4b	2025-11-05	Warnings	Exact identifier application number: M007
up and up gentle laxative	BISACODYL	Target Corporation	4a29dc2b-b68f-471b-a84e-4a5096aa3748	2025-11-04	Warnings	Exact identifier application number: M007
Target Fiber Laxative	PSYLLIUM HUSK	TARGET CORPORATION	a581116a-392d-4ac3-ae15-4318506a7b2a	2025-11-04	Warnings	Exact identifier application number: M007
up and up fiber therapy	CALCIUM POLYCARBOPHIL	Target Corporation.	e5473950-06f4-4ea4-975b-3ac94957e776	2025-11-04	Warnings	Exact identifier application number: M007
up and up fiber therapy Natural Fiber	PSYLLIUM HUSK	Target Corporation	f8b1c831-6fd0-4a58-9726-4e0f986c8084	2025-11-04	Warnings	Exact identifier application number: M007
OneLAX	BISACODYL	AKRON PHARMA INC	be4eeb4d-df29-45dc-94ff-933e52c8b6f6	2025-11-03	Warnings	Exact identifier application number: M007
Gentle Stool Softener	DOCUSATE SODIUM	WALGREEN COMPANY	169b33f9-e559-47bf-bbba-c7eda4762c7f	2025-10-31	Warnings	Exact identifier application number: M007
Senna S	DOCUSATE SODIUM, SENNOSIDES	Walgreens	765bfd9b-7a21-4315-9add-cf13007722d5	2025-10-31	Warnings	Exact identifier application number: M007
Gentle Stool Softener	DOCUSATE SODIUM	WALGREEN COMPANY	71b15339-2585-4fae-8445-6fbb4f0a378e	2025-10-31	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Major Pharmaceuticals	97561cd4-63d9-44c2-a3a3-ec668a09a4ed	2025-10-31	Warnings	Exact identifier application number: M007
Fiber Caplets	CALCIUM POLYCARBOPHIL	SAFEWAY	08e2e8b0-90b3-48d6-a72a-40688c74771a	2025-10-29	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN	Chain Drug Marketing Association Inc.	424d91f0-ecf9-6d9b-e063-6394a90a8006	2025-10-29	Warnings	Exact identifier application number: M007
Publix Laxative Maximum Strength	CALCIUM SENNOSIDES	PUBLIX SUPER MARKETS, INC	11112859-ef1e-4b37-9915-ba4d06a3f198	2025-10-28	Warnings	Exact identifier application number: M007
Publix Stimulant Laxative	BISACODYL	PUBLIX SUPER MARKETS, INC	02e596a7-b8e5-4f55-9bc6-6d17e0fabda7	2025-10-28	Warnings	Exact identifier application number: M007
PUBLIX	PSYLLIUM HUSK	PUBLIX SUPER MARKETS, INC	55f98d3f-f282-4f19-b373-0b59640d274d	2025-10-28	Warnings	Exact identifier application number: M007
PUBLIX	CALCIUM POLYCARBOPHIL	PUBLIX SUPER MARKETS, INC	02e3f4ce-8961-425c-98a9-3b9d66709ca5	2025-10-28	Warnings	Exact identifier application number: M007
Publix Women Laxative	BISACODYL	PUBLIX SUPER MARKETS, INC	03eeca55-f239-4a01-a900-c1943f27a834	2025-10-28	Warnings	Exact identifier application number: M007
Publix Fiber Therapy Orange Smooth	PSYLLIUM HUSK	PUBLIX SUPER MARKETS, INC	b9c54c20-cd82-4627-9217-a66834db4799	2025-10-28	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

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1115005	docusate sodium 100 MG Oral Capsule	PSN	4658d162-6e62-4d84-b5d6-7bf16c915558	5
1115005	docusate sodium 100 MG Oral Capsule	SCD	4658d162-6e62-4d84-b5d6-7bf16c915558	5
1115005	DOSS Sodium 100 MG Oral Capsule	SY	4658d162-6e62-4d84-b5d6-7bf16c915558	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0113-0486-72	00113048672	1 BOTTLE in 1 CARTON (0113-0486-72) > 60 CAPSULE, LIQUID FILLED in 1 BOTTLE	1 bottle	1991-10-29	0000-00-00	No	No	Current
0113-0486-78	00113048678	100 CAPSULE, LIQUID FILLED in 1 BOTTLE (0113-0486-78)		2025-08-14		No	No	Current