Womens Gentle Laxative

Product NDC: 21130-555
11-digit product format: 211300555
Labeler code: 21130
Product ID: 21130-555_2dede456-ed44-095a-e063-6294a90aff1e
Type: HUMAN OTC DRUG
Nonproprietary name: Bisacodyl
Dosage form: TABLET
Route: ORAL
Labeler: BETTER LIVING BRANDS LLC.
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2023-07-10
Substance: BISACODYL
Active strength: 5 mg/1
Pharmacologic classes: Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
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	21130-555		D	Discontinued by firm		2026-10-15
excluded package	package	21130-555	21130-555-01	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 · 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	21130-555-01	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	21130-555-01	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	21130-555-01	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	21130-555-01	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	21130-555-01	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	21130-555-01	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
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	21130-555-30	U	Excluded because listing certification expired	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	21130-555-01	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
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	21130-555-30	U	Excluded because listing certification expired	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	21130-555-01	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
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	21130-555-30	U	Excluded because listing certification expired	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	21130-555-01	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	21130-555-01	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	21130-555-01	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	21130-555-01	D	Discontinued by firm	`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: Womens Gentle Laxative
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BISACODYL	5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
10X0709Y6I	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
308753	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
f2c4ed1a-5aa4-1915-e053-2a95a90a59b6	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6	Product name	1	20230320
11ed6f83-cdd2-4637-8379-b1a1d3ae3cde	Product name	1	20181101
86c45a79-b9f0-4476-a27c-6e10db098497	Product name	1	20180125
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
21130-555-30	2025-02-12	C162847	48780-1	2cef2736-9f9f-d83d-e063-dadaa90ab31f	151R_Albertsons_21130-555_Bisacodyl USP 5 mg-stimulant laxative
21130-555-30	2025-01-30	C162847	48780-1	2cef2736-9f9f-d83d-e063-dadaa90ab31f	151R_Albertsons_21130-555_Bisacodyl USP 5 mg-stimulant laxative

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
21130-555-30	Womens Gentle Laxative	15 in 1 BLISTER PACK	TABLET	15		3
21130-555-30	Womens Gentle Laxative	2 in 1 CARTON	TABLET	2		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
21130-555	WOMENS GENTLE LAXATIVE (BISACODYL) TABLET [BETTER LIVING BRANDS LLC.]	3	Current NDC, 2 package rows	20250214_f2c4ed1a-5aa4-1915-e053-2a95a90a59b6.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 17 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DDM Castor Oil	CASTOR OIL	Discount Drug Mart	5d1583fa-968a-5987-e053-2991aa0a0d60	2025-12-19	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	P & L Development, LLC	cb0765cb-f48e-4daa-97b8-2897a2d95587	2025-12-19	Warnings	Exact identifier application number: M007
Humco Castor Oil	CASTOR OIL	Humco holding Group, Inc.	f2676cf2-f6fb-46b8-b723-5497f1655902	2025-12-18	Warnings	Exact identifier application number: M007
Humco Castor Oil (Regular)	CASTOR OIL	Humco Holding Group, Inc.	ccf25c1f-d8a2-49b9-8e09-88e6616c9ade	2025-12-18	Warnings	Exact identifier application number: M007
Meijer Magnesium Hydroxide Laxative Soft Chew	MAGNESIUM HYDROXIDE	Meijer	23f826c3-1ad5-b3c8-e063-6394a90a655e	2025-12-18	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Strategic Sourcing Services LLC	ba51cca1-b70b-476e-80e6-20cd52292e65	2025-12-17	Warnings	Exact identifier application number: M007
Stool Softener Extra Strength	DOCUSATE SODIUM	CVS Pharmacy	a694b4f3-6112-4a1d-a06e-9e5b20fd3d7b	2025-12-17	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	CARDINAL HEALTH 110, LLC. DBA LEADER 70000	da5ccd75-8a2f-4f90-ae8a-97d81b8579d2	2025-12-17	Warnings	Exact identifier application number: M007
Sennosides	SENNOSIDES	Morepen Laboratories Limited	3643eabf-e339-f02c-e063-6394a90aa6a8	2025-12-16	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Meijer Distribution Inc	f425a7aa-2503-2fe8-e053-2995a90ab352	2025-12-16	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Meijer Distribution Inc.	f42591f9-c842-018f-e053-2995a90a480f	2025-12-16	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA ORIGINAL	MAGNESIUM HYDROXIDE	MAJOR Pharmaceuticals Inc.	673311f7-0b83-410c-a480-8e57d0190296	2025-12-11	Warnings	Exact identifier application number: M007
GeriCare Docusate Sodium Liquid	DOCUSATE SODIUM	GERI-CARE PHARMACEUTICALS, CORP	d599ff49-c9a4-401a-a50b-63d89749bbed	2025-12-11	Warnings	Exact identifier application number: M007
GeriCare Senna Syrup	SENNOSIDES	Geri-Care Pharmaceutical Corp.	05a54614-a6ad-4861-87b8-9e2ee49bad20	2025-12-11	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	Major Pharmaceuticals	3e8321cf-7eda-d70c-e063-6394a90a35a5	2025-12-10	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	HEB	2f103a88-4cab-d4b9-e063-6394a90ac7fc	2025-12-09	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	HEB	2efb4c5a-2c5e-acf6-e063-6394a90a934e	2025-12-08	Warnings	Exact identifier application number: M007
Stool Softener	DOCUSATE SODIUM	HEB	2f10041a-8c88-09a5-e063-6294a90a07cc	2025-12-08	Warnings	Exact identifier application number: M007
QUALITY CHOICE Fiber Therapy	METHYLCELLULOSE	CHAIN DRUG MARKETING ASSOCIATION	77ac079c-d957-4706-8241-570d7fcfe3aa	2025-12-04	Warnings	Exact identifier application number: M007
Phillips Stool Softener Bulk Docusate	DOCUSATE SODIUM	Bayer HealthCare LLC.	b0462555-5554-4a17-a1fe-4206a4fd350d	2025-12-04	Warnings	Exact identifier application number: M007

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
10X0709Y6I	BISACODYL	603-50-9	BISACODYL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
308753	bisacodyl 5 MG Delayed Release Oral Tablet	PSN	f2c4ed1a-5aa4-1915-e053-2a95a90a59b6	3
308753	bisacodyl 5 MG Delayed Release Oral Tablet	SCD	f2c4ed1a-5aa4-1915-e053-2a95a90a59b6	3
308753	bisacodyl 5 MG Enteric Coated Oral Tablet	SY	f2c4ed1a-5aa4-1915-e053-2a95a90a59b6	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
21130-555-30	21130055530	2 BLISTER PACK in 1 CARTON (21130-555-30) / 15 TABLET in 1 BLISTER PACK	2 blister pack	2023-07-10	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
151R_Albertsons_21130-555_Bisacodyl USP 5 mg-stimulant laxative	BETTER LIVING BRANDS LLC. \| TIME CAP LABORATORIES, INC.	2025-02-12	HUMAN OTC DRUG LABEL	3