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 38 of 42 · 829 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Stool Softener Laxative	DOCUSATE SODIUM	BJWC (Berkley & Jensen / BJ's)	2ca80e23-f38a-4f77-b536-131cc9f0cf5b	2024-02-23	Warnings	Exact identifier application number: M007
Colon Detox	DOCUSATE SODIUM AND SENNOSIDES	OPMX LLC	0a4d3265-080c-d2ed-e063-6394a90adbee	2024-02-21	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM AND SENNOSIDES	Best Choice (Valu Merchandisers Company)	4501d718-15a7-4e27-bdb1-8aa2d3ff06d0	2024-02-20	Warnings	Exact identifier application number: M007
Stool Softener Laxative	DOCUSATE SODIUM	Best Choice (Valu Merchandisers Company)	72bd251b-4e82-41ef-8362-39f95faf9916	2024-02-15	Warnings	Exact identifier application number: M007
Magnesium Citrate	LEADER MAGNESIUM CITRATE ORAL SOLUTION - LEMON	CARDINAL HEALTH, INC. 063997360	10bdd5e6-3db2-8f9e-e063-6394a90a9b3f	2024-02-06	Warnings	Exact identifier application number: M007
Magnesium Citrate	LEADER MAGNESIUM CITRATE ORAL SOLUTION - GRAPE	CARDINAL HEALTH, INC. 063997360	10beb3ec-a189-221d-e063-6394a90aabb5	2024-02-06	Warnings	Exact identifier application number: M007
Magnesium Citrate	LEADER MAGNESIUM CITRATE ORAL SOLUTION - CHERRY	CARDINAL HEALTH, INC. 063997360	10bebb63-19b3-2e14-e063-6394a90a8d4e	2024-02-06	Warnings	Exact identifier application number: M007
Docusate Sodium	DOCUSATE SODIUM	Proficient Rx LP	f9ac0344-5864-4ac1-81bc-16878a5946c5	2024-02-01	Warnings	Exact identifier application number: M007
Purifi Hand Sanitizer	BENZALKONIUM CHLORIDE	Purifi LLC	9267069d-4cf5-4e48-a446-7dbebea16bf5	2024-01-31	Warnings	Exact identifier application number: M007
WOMENS LAXATIVE ENTERIC COATED	BISACODYL	CARDINAL HEALTH	ab34bc89-6738-d284-e053-2a95a90a5dc9	2024-01-11	Warnings	Exact identifier application number: M007
MAXIMUM STRENGTH LAXATIVE	SENNOSIDES	CARDINAL HEALTH	b7b13bfa-8a94-6f62-e053-2995a90abbf4	2024-01-10	Warnings	Exact identifier application number: M007
FIBER LAXATIVE	CALCIUM POLYCARBOPHIL	Magno-Humphries, Inc.	e4a921c5-1cf7-12ca-e053-2a95a90a6e04	2024-01-03	Warnings	Exact identifier application number: M007
Freskaro Castor Oil	CASTOR OIL	Pharma Nobis, LLC	fbd6bdd5-a7a1-3f28-e053-6294a90aab87	2023-12-28	Warnings	Exact identifier application number: M007
Humco Castor Oil	CASTOR OIL	Pharma Nobis, LLC	e42f9d37-1b07-177a-e053-2a95a90a9b06	2023-12-26	Warnings	Exact identifier application number: M007
Magnesium Citrate	FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - LEMON	Pharma Nobis, LLC	f0477328-eca1-9043-e053-2995a90aaa3d	2023-12-22	Warnings	Exact identifier application number: M007
Magnesium Citrate	FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - CHERRY	Pharma Nobis, LLC	f0489f6f-9e60-7d69-e053-2a95a90a9dfb	2023-12-22	Warnings	Exact identifier application number: M007
Magnesium Citrate	FRESKARO MAGNESIUM CITRATE ORAL SOLUTION - GRAPE	Pharma Nobis, LLC	f0488c86-6c74-3987-e053-2a95a90a31b4	2023-12-22	Warnings	Exact identifier application number: M007
Mineral Oil Heavy	MINERAL OIL	Pharma Nobis, LLC	e42f6c6d-c4de-02c6-e053-2995a90a3ace	2023-12-22	Warnings	Exact identifier application number: M007
Quality Choice Castor Oil	CASTOR OIL	Chain Drug Market Asociation	18d7124f-7745-45b2-adc4-cb1103add5d6	2023-12-20	Warnings	Exact identifier application number: M007
Premiere Value Castor Oil	CASTOR OIL	Chain Drug Consortium	5c8c1564-fcff-894b-e053-2991aa0a9c0b	2023-12-20	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