Bisacodyl

Product NDC: 0904-7142
11-digit product format: 009047142
Labeler code: 0904
Product ID: 0904-7142_41e9e0e3-789c-6224-e063-6394a90aa58e
Type: HUMAN OTC DRUG
Nonproprietary name: Bisacodyl
Dosage form: SUPPOSITORY
Route: RECTAL
Labeler: Major Pharmaceuticals
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-05-05
Substance: BISACODYL
Active strength: 10 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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	0904-7142	0904-7142-60	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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`

Additional Listing Data#

Finished product: Yes
Brand name base: Bisacodyl
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BISACODYL	10 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
198509	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
c194c40c-c732-2f03-e053-2a95a90a7a40	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0904-7142-12	Bisacodyl	2 in 1 CARTON	SUPPOSITORY	2	5
0904-7142-12	Bisacodyl	6 in 1 BLISTER PACK	SUPPOSITORY	6	5
0904-7142-60	Bisacodyl	100 in 1 CARTON	SUPPOSITORY	100	5
0904-7142-60	Bisacodyl	1 in 1 BLISTER PACK	SUPPOSITORY	1	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0904-7142-12	EA - Each	0904-7142	30183eff-b6ea-4f0a-89a3-d740e8735e9f	1	2021-10-08
0904-7142-60	EA - Each	0904-7142	7a45acd3-c30c-454b-811d-83fb543085bc	1	2021-10-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0904-7142	BISACODYL (BISACODYL) SUPPOSITORY [MAJOR PHARMACEUTICALS]	4	Current NDC, Legacy NDC, 4 package rows	20241215_c194c40c-c732-2f03-e053-2a95a90a7a40.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 · 878 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
10X0709Y6I	BISACODYL	603-50-9	BISACODYL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198509	bisacodyl 10 MG Rectal Suppository	PSN	c194c40c-c732-2f03-e053-2a95a90a7a40	5
198509	bisacodyl 10 MG Rectal Suppository	SCD	c194c40c-c732-2f03-e053-2a95a90a7a40	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0904-7142-12	00904714212	2 BLISTER PACK in 1 CARTON (0904-7142-12) / 6 SUPPOSITORY in 1 BLISTER PACK	2 blister pack	2021-05-05	0000-00-00	No	No	Current
0904-7142-60	00904714260	100 BLISTER PACK in 1 CARTON (0904-7142-60) > 1 SUPPOSITORY in 1 BLISTER PACK	100 blister pack	2021-05-05	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Major Bisacodyl Suppositories	Major Pharmaceuticals \| DSC Laboratories, Inc.	2025-10-24	HUMAN OTC DRUG LABEL	5