Stool Softener

Product NDC: 30142-407
11-digit product format: 301420407
Labeler code: 30142
Product ID: 30142-407_08649f4b-9276-f53f-e063-6394a90a023a
Type: HUMAN OTC DRUG
Nonproprietary name: Docusate Sodium
Dosage form: CAPSULE, LIQUID FILLED
Route: ORAL
Labeler: KROGER COMPANY
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-03-01
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	30142-407		D	Discontinued by firm		2026-09-14
excluded package	package	30142-407	30142-407-01	D	Discontinued by firm		2026-09-14

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 · 30 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	30142-407-01	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	30142-407-01	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	30142-407-01	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	30142-407-01	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	30142-407-01	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	30142-407-01	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	30142-407-01	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	30142-407-01	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	30142-407-01	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	30142-407-01	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	30142-407-01	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	30142-407-01	D	Discontinued by firm	`557ba5c1ecfa…`	`9c80585c8c6e…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	30142-407-01	I	Inactivated by FDA	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	30142-407-01	I	Inactivated by FDA	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	30142-407-01	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`

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: 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
a1afaa71-7e8c-5a49-e053-2a95a90a4db0	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
30142-407-01	2022-11-17	C162847	48780-1	d6a99b39-e336-a426-e053-dadaa90af4c2	kro 406
30142-407-01	2022-01-28	C162847	48780-1	d6a99b39-e336-a426-e053-dadaa90af4c2	kro 406

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
30142-407-01	Stool Softener	100 in 1 BOTTLE	CAPSULE, LIQUID FILLED	100		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
30142-407	STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [KROGER COMPANY]	4	Current NDC, Legacy NDC, 1 package rows	20231024_a1afaa71-7e8c-5a49-e053-2a95a90a4db0.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 · 865 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	a1afaa71-7e8c-5a49-e053-2a95a90a4db0	4
1115005	docusate sodium 100 MG Oral Capsule	SCD	a1afaa71-7e8c-5a49-e053-2a95a90a4db0	4
1115005	DOSS Sodium 100 MG Oral Capsule	SY	a1afaa71-7e8c-5a49-e053-2a95a90a4db0	4

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
30142-407-01	30142040701	100 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-407-01)	2020-03-01	0000-00-00	No	No	Current