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 26 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Womens Gentle Laxative	BISACODYL	BETTER LIVING BRANDS LLC.	f2c4ed1a-5aa4-1915-e053-2a95a90a59b6	2025-02-12	Warnings	Exact identifier application number: M007
Laxative	SENNOSIDES	BETTER LIVING BRANDS LLC.	f2c5c1e6-3123-c802-e053-2995a90aa073	2025-02-12	Warnings	Exact identifier application number: M007
Vegetable Laxative	SENNOSIDES	BETTER LIVING BRANDS LLC.	f2c529e4-6738-377c-e053-2995a90aaf38	2025-02-12	Warnings	Exact identifier application number: M007
WOMENS GENTLE LAXATIVE	BISACODYL	CVS HEALTH CORP	a95073f3-e1d6-d291-e053-2a95a90aefea	2025-02-12	Warnings	Exact identifier application number: M007
MAXIMUM STRENGTH LAXATIVE	SENNOSIDES	CVS HEALTH	b05ee52f-4801-d4ca-e053-2995a90af348	2025-02-12	Warnings	Exact identifier application number: M007
SENNA	SENNOSIDES	Reliable 1 Laboratories LLC	c8aa7ae9-7d00-db7d-e053-2995a90ae72b	2025-02-11	Warnings	Exact identifier application number: M007
Extra Gentle Laxative	BISACODYL	DOLGENCORP INC	be214c4e-f6db-cc8d-e053-2a95a90addf7	2025-02-10	Warnings	Exact identifier application number: M007
SENNA-S	DOCUSATE SODIUM AND SENNOSIDES	KROGER	a187045c-c9d6-592a-e053-2995a90adb83	2025-02-10	Warnings	Exact identifier application number: M007
SENNA TIME	SENNOSIDES	TIME CAP LABORATORIES, INC	18ec8127-422c-4c1a-8331-58dabce69969	2025-02-08	Warnings	Exact identifier application number: M007
SENNA TIME S	DOCUSATE SODIUM-SENNOSIDES	TIME CAP LABORATORIES, INC	dc491692-8d3a-4ccd-a17d-4c630f122595	2025-02-08	Warnings	Exact identifier application number: M007
LAX-TIME	SENNOSIDES	TIME CAP LABORATORIES, INC	74a627fc-00e5-eb78-e053-2991aa0abacc	2025-02-08	Warnings	Exact identifier application number: M007
SENNOSIDES AND DOCUSATE SODIUM	SENNOSIDES AND DOCUSATE SODIUM	TIME CAP LABORATORIES, INC	0ad617e0-10a6-44fa-be62-4f3cc725fb01	2025-02-08	Warnings	Exact identifier application number: M007
Sennosides and Docusate Sodium	SENNOSIDES, DOCUSATE SODIUM	Asclemed USA, Inc.	2db546de-20dc-4697-aff2-12471f073b1d	2025-02-08	Warnings	Exact identifier application number: M007
SENNOSIDES	SENNOSIDES	TIME CAP LABORATORIES, INC	7498f5fa-1739-bb6e-e053-2a91aa0a5404	2025-02-07	Warnings	Exact identifier application number: M007
Gentle Laxative	MAGNESIUM HYDROXIDE	WALMART INC.	26b9f247-c242-2925-e063-6394a90a68dd	2025-02-06	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	PAI Holdings, LLC dba PAI Pharma	e975a3f1-0e1f-4fb8-9c5f-baa75e12f2a5	2025-02-06	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	PD-Rx Pharmaceuticals, Inc.	6a7e4193-22d2-491e-9842-5c43f571fc65	2025-02-05	Warnings	Exact identifier application number: M007
Mineral oil	MINERAL OIL	Best Choice (Valu Merchandisers Company)	3ec8a716-60e0-4dfb-adae-ddc53c613935	2025-02-04	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM 50MG SOFTGEL (RED)	DOCUSATE SODIUM	CVS Pharmacy	273e5b52-1cf9-2525-e063-6394a90a8b4f	2025-02-04	Warnings	Exact identifier application number: M007
Laxative	SENNOSIDES	WALGREENS	f0caba1d-0c09-8496-e053-2995a90a47cf	2025-01-30	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