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		2026-10-16
excluded package	package	21130-555	21130-555-01	D	Discontinued by firm		2026-10-16

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 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
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