Walgreens Gentle Laxative

Product NDC: 0363-0466
11-digit product format: 003630466
Labeler code: 0363
Product ID: 0363-0466_485ea50e-b62b-cbb9-e063-6394a90a1cdf
Type: HUMAN OTC DRUG
Nonproprietary name: Bisacodyl Suppository
Dosage form: SUPPOSITORY
Route: RECTAL
Labeler: Walgreens
Application: M007
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-09-18
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: 2027-12-31
Current FDA listing: Yes

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 · 14 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
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	0363-0466-31	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	0363-0466-31	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	0363-0466-31	I	Inactivated by FDA	`bd6a592717d7…`	`303034d00443…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	0363-0466-31	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	0363-0466-09	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded product	product		E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	0363-0466-31	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`
2019-12-08 06:16 UTC · source 2019-12-05	excluded package	package	0363-0466-09	E	Excluded after deficient or non-compliant submission was not corrected	`110d247fa046…`	`a55b01930146…`

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: Walgreens Gentle Laxative
Listing expiration: 2027-12-31

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
d094ba43-7404-43c4-b907-41ab6d02a3c3	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, Indexing SPL table
NDC	Effective	Indexing SPL	Related label
0363-0466-31	2022-12-19	9d75b9d0-15b2-f424-e053-dadaa90a57ce	Walgreens ® Gentle Laxative 30ct
0363-0466-31	2022-01-28	9d75b9d0-15b2-f424-e053-dadaa90a57ce	Walgreens ® Gentle Laxative 30ct
0363-0466-09	2020-11-03	9d75b9d1-279c-f424-e053-dadaa90a57ce	Walgreens ® Gentle Laxative 8ct
0363-0466-31	2020-11-03	9d75b9d0-15b2-f424-e053-dadaa90a57ce	Walgreens ® Gentle Laxative 30ct
0363-0466-09	2020-01-31	9d75b9d1-279c-f424-e053-dadaa90a57ce	Walgreens ® Gentle Laxative 8ct
0363-0466-31	2020-01-31	9d75b9d0-15b2-f424-e053-dadaa90a57ce	Walgreens ® Gentle Laxative 30ct

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0363-0466-08	Walgreens Gentle Laxative	2 in 1 PACKAGE	SUPPOSITORY	2	7
0363-0466-08	Walgreens Gentle Laxative	4 in 1 BLISTER PACK	SUPPOSITORY	4	7
0363-0466-04	Walgreens Gentle Laxative	4 in 1 BLISTER PACK	SUPPOSITORY	4	6
0363-0466-04	Walgreens Gentle Laxative	1 in 1 PACKAGE	SUPPOSITORY	1	6
0363-0466-30	Walgreens Gentle Laxative	5 in 1 PACKAGE	SUPPOSITORY	5	6
0363-0466-30	Walgreens Gentle Laxative	6 in 1 CARTRIDGE	SUPPOSITORY	6	6

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0363-0466-08	EA - Each	0363-0466	48dc80d4-fd27-476d-9e73-ba1db087052b	1	2016-07-19

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-0466	WALGREENS GENTLE LAXATIVE (BISACODYL SUPPOSITORY) SUPPOSITORY [WALGREENS]	6	Current NDC, Legacy NDC, 2 package rows	20241227_d094ba43-7404-43c4-b907-41ab6d02a3c3.zip
0363-0466	WALGREENS GENTLE LAXATIVE (BISACODYL SUPPOSITORY) SUPPOSITORY [WALGREENS]	5	Current NDC, Legacy NDC, 2 package rows	20241227_015e41d2-7543-4210-8345-626f5ae5f81d.zip
0363-0466	WALGREENS GENTLE LAXATIVE (BISACODYL SUPPOSITORY) SUPPOSITORY [WALGREENS]	5	Current NDC, Legacy NDC, 2 package rows	20241227_2c30de62-b5d2-4905-90a1-a2f9a339fb27.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 5 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MILK OF MAGNESIA MINT	MAGNESIUM HYDROXIDE	Preferred Pharmaceuticals Inc.	f8bba8cb-a111-4285-8bdb-2273a049c3bb	2026-07-08	Warnings	Exact identifier application number: M007
DOCUSATE SODIUM, EXTRA STRENGTH 250 MG	DOCUSATE SODIUM	Advanced Rx LLC	fc8cf24e-8ca1-b3fb-e053-6294a90a7a50	2026-07-06	Warnings	Exact identifier application number: M007
Curewell Docusate Sodium Liquid	DOCUSATE SODIUM.50MG/5ML	RMT HEALTH LLC	55903043-2a1d-0525-e063-6394a90ae182	2026-07-01	Warnings	Exact identifier application number: M007
Senna	SENNOSIDES 8.6 MG TABLETS	Aarkish Pharmaceuticals NJ Inc.	564bc9a5-13b5-4cce-a349-6b2e122683ed	2026-07-01	Warnings	Exact identifier application number: M007
Senna-S	DOCUSATE SODIUM 50 MG SENNOSIDES 8.6 MG	Aarkish Pharmaceuticals NJ Inc.	faca8f3e-d9eb-44c5-93ab-f59ed1c0f56f	2026-07-01	Warnings	Exact identifier application number: M007
ENEMEEZ	DOCUSATE SODIUM	Quest Products, LLC	0b06445d-0839-497e-bdff-e0fe224a7738	2026-06-30	Warnings	Exact identifier application number: M007
ENEMEEZ Plus	DOCUSATE SODIUM AND BENZOCAINE	Quest Products, LLC	1670ca59-7275-4ac6-bef4-674a7b24c7b3	2026-06-30	Warnings	Exact identifier application number: M007
Mineral oil	MINERAL OIL	CVS Pharmacy, Inc.	1183bcbc-51ec-e53a-e063-6394a90af0f2	2026-06-26	Warnings, Adverse reactions	Exact identifier application number: M007
Glycerin	GLYCERIN	Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd	552d9018-cc7d-7e1a-e063-6294a90a3322	2026-06-26	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN	Beijing Jingfeng Pharmaceutical (Shandong) Co., Ltd	552e16b9-f46a-7838-e063-6394a90ab8aa	2026-06-26	Warnings	Exact identifier application number: M007
Walgreens Gentle Laxative	BISACODYL SUPPOSITORY	Walgreens	20c43036-830b-0e1d-e063-6394a90adf5f	2026-06-25	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	American Health Packaging	be7cab51-ce7e-465d-95db-083e69288cfd	2026-06-25	Warnings	Exact identifier application number: M007
Epsom Salt	MAGNESIUM SULFATE	Vi-Jon, LLC	ba490c22-19f0-4887-9509-bd3d32e0f5b1	2026-06-24	Warnings, Adverse reactions	Exact identifier application number: M007
MILK OF MAGNESIA	MAGNESIUM HYDROXIDE	KROGER COMPANY	a1b0c638-6c34-1b72-e053-2995a90acc85	2026-06-24	Warnings	Exact identifier application number: M007
Womens Laxative	WOMENS LAXTIVE	Allegiant Health	549a11d1-a096-4c22-96b4-2d4f54f46022	2026-06-24	Warnings	Exact identifier application number: M007
Magnesium Citrate	MAGNESIUM CITRATE	Meijer Distribution Inc	f4259fda-19d4-087e-e053-2995a90a7081	2026-06-22	Warnings	Exact identifier application number: M007
STOOL SOFTENER	DOCUSATE SODIUM	Geri-Care Pharmaceuticals, Corp	3ec42148-6786-22f2-e054-00144ff8d46c	2026-06-18	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN SUPPOSITORY	Everpharm LLC	546347e5-841e-15ca-e063-6294a90a0c8b	2026-06-16	Warnings	Exact identifier application number: M007
Glycerin	GLYCERIN SUPPOSITORY	Everpharm LLC	5463f869-2b92-4551-e063-6394a90ad6f9	2026-06-16	Warnings	Exact identifier application number: M007
MINICA-S	GLYCERIN	Sato Pharmaceutical Co., Ltd.	687902eb-e702-4e87-a0ce-9add05e3cbc1	2026-06-16	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
198509	bisacodyl 10 MG Rectal Suppository	PSN	d094ba43-7404-43c4-b907-41ab6d02a3c3	7
198509	bisacodyl 10 MG Rectal Suppository	SCD	d094ba43-7404-43c4-b907-41ab6d02a3c3	7
198509	bisacodyl 10 MG Rectal Suppository	PSN	015e41d2-7543-4210-8345-626f5ae5f81d	6
198509	bisacodyl 10 MG Rectal Suppository	PSN	2c30de62-b5d2-4905-90a1-a2f9a339fb27	6
198509	bisacodyl 10 MG Rectal Suppository	SCD	015e41d2-7543-4210-8345-626f5ae5f81d	6
198509	bisacodyl 10 MG Rectal Suppository	SCD	2c30de62-b5d2-4905-90a1-a2f9a339fb27	6

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0363-0466-04	00363046604	1 BLISTER PACK in 1 PACKAGE (0363-0466-04) / 4 SUPPOSITORY in 1 BLISTER PACK	1 blister pack	2020-11-04	0000-00-00	No	No	Current
0363-0466-08	00363046608	2 BLISTER PACK in 1 PACKAGE (0363-0466-08) / 4 SUPPOSITORY in 1 BLISTER PACK	2 blister pack	2014-09-18		No	No	Current
0363-0466-09	00363046609	2 BLISTER PACK in 1 PACKAGE (0363-0466-09) > 40 mg in 1 BLISTER PACK (0363-0466-08)	2 blister pack	2014-09-18	0000-00-00	No	No	Current
0363-0466-30	00363046630	5 CARTRIDGE in 1 PACKAGE (0363-0466-30) / 6 SUPPOSITORY in 1 CARTRIDGE	5 cartridge	2014-09-18		No	No	Current
0363-0466-31	00363046631	5 CARTRIDGE in 1 PACKAGE (0363-0466-31) > 60 mg in 1 CARTRIDGE (0363-0466-30)	5 cartridge	2014-09-18	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Walgreens ® Gentle Laxative 8ct	Walgreens \| Unipack LLC	2026-01-15	HUMAN OTC DRUG LABEL	7
Walgreens ® Gentle Laxative 30ct	Walgreens \| Unipack LLC	2026-01-15	HUMAN OTC DRUG LABEL	6
Walgreens ® Gentle Laxative 4ct	Walgreens \| Unipack LLC	2026-01-15	HUMAN OTC DRUG LABEL	6