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 19 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stool Softener Laxative	DOCUSATE SODIUM	The Kroger Co.	9019ae9e-da3e-4ed1-b83e-d9a6375e9c30	2025-11-25	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Family Dollar (FAMILY WELLNESS)	d61ba4ef-5b03-4d29-b1fd-81591f0c8a2c	2025-11-25	Warnings	Exact identifier application number: M007
Senna S	DOCUSATE SODIUM AND SENNOSIDES	Marlex Pharmaceuticals Inc	9c87759f-3856-4f30-b5ea-4b37ed90f18c	2025-11-21	Warnings	Exact identifier application number: M007
Sennosides	SENNOSIDES	Marlex Pharmaceuticals Inc	5ca287a3-c4f6-402d-978e-cd1328bdbc47	2025-11-21	Warnings	Exact identifier application number: M007
SAMS WEST	PSYLLIUM HUSK	SAM'S WEST INC	2aaf5d99-6d28-4fa6-b3c5-52dcfc94dac0	2025-11-20	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA ORIGINAL	MAGNESIUM HYDROXIDE	Geri-Care Pharmaceuticals, Corp	bb47ad1f-251c-491e-8ddd-6f6f719efa15	2025-11-20	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA ORIGINAL	MAGNESIUM HYDROXIDE	Chain Drug Marketing Association	440a96bb-9e68-bdcc-e063-6294a90a6793	2025-11-20	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA ORIGINAL	MAGNESIUM HYDROXIDE	Chain Drug Marketing Association	4277b174-4ce5-4950-8e9b-75e3c019a8f3	2025-11-20	Warnings	Exact identifier application number: M007
Fleet	SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC	C.B. Fleet Company, Inc.	c1677d70-203b-493e-88f0-815a66133f1d	2025-11-20	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	FAMILY DOLLAR SERVICES INC	5ea9237a-7895-388d-e053-2991aa0a92b0	2025-11-19	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	FAMILY DOLLAR SERVICES INC	5ea9305b-2997-49d3-e053-2991aa0a1fa1	2025-11-19	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	CVS	3c8f5b69-56f2-4e9d-e054-00144ff88e88	2025-11-19	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	CVS	3cdf1975-2607-14f5-e054-00144ff8d46c	2025-11-19	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	RITE AID PHARMACY	60284706-445f-f795-e053-2a91aa0a0a12	2025-11-19	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA CHERRY	MAGNESIUM HYDROXIDE	Geri-Care Pharmaceuticals, Corp	9f588e9b-56c5-4426-89fc-7b83e2d0ad1a	2025-11-19	Warnings	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	Fact Products	aebbdd10-0650-6efe-e053-2a95a90a0ab2	2025-11-19	Warnings	Exact identifier application number: M007
Stool Softener with Stimulant Laxative	DOCUSATE SODIUM AND SENNOSIDES	P & L Development, LLC	0cbe3b61-ce35-4be1-9caf-9c61fce10ca2	2025-11-17	Warnings	Exact identifier application number: M007
good sense stool softener	DOCUSATE SODIUM	L. Perrigo Company	4658d162-6e62-4d84-b5d6-7bf16c915558	2025-11-14	Warnings	Exact identifier application number: M007
Topco Fiber Therapy Sugar Free	PSYLLIUM HUSK	TOPCO ASSOCIATES LLC	2c61e73e-b3f7-4ab2-8bda-e65a2c0b3560	2025-11-10	Warnings	Exact identifier application number: M007
Calcium Polycarbophil	CALCIUM POLYCARBOPHIL	LEADER/ Cardinal Health 110, Inc.	b4637e18-c65f-0e81-e053-2a95a90a2284	2025-11-06	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