Fleet
- Product NDC
- 0132-0401
- 11-digit product format
- 001320401
- Labeler code
- 0132
- Product ID
- 0132-0401_4340697d-d634-493f-8b79-cdf7a1b30fff
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- bisacodyl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- C.B. Fleet Company, Inc.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-21
- 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
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
- Fleet
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| BISACODYL | 5 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 10X0709Y6I | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 308753 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4e0d973f-e6dc-48d9-8df3-1d47c87840f1 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| fb7ab793-2c12-4079-b100-a64f73bef25a | Product name | 4 | 20240712 |
| b0cbf770-6cc3-4aa4-9158-755110c2b9f7 | Product name | 2 | 20230717 |
| dc7c5daa-021f-40dd-b00d-63982cb2067a | Product name | 1 | 20230426 |
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 5 | 20200925 |
| 816b97af-edc5-4060-aff1-b814bdbcad50 | Product name | 1 | 20190415 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 7cda52fc-125f-421c-8fea-bc1974370c49 | Product name | 2 | 20180703 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| 419aab54-5d5a-4146-9453-026d4a9991be | Product name | 2 | 20170525 |
| 08ffbcbf-26df-b99c-1dab-64fc4cfae89f | Product name | 2 | 20160823 |
| 89dac932-b90a-4410-9ab1-84c53e57de25 | Product name | 1 | 20150316 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0132-0401-25 | Fleet | 25 in 1 BLISTER PACK | TABLET, COATED | 25 | 1 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Senna Syrup | NATURAL VEGETABLE LAXATIVE | Bryant Ranch Prepack | 2c0d62e7-563b-46e4-9793-183e98e761a6 | 2026-03-25 | Warnings | M007 |
| Laxomil | BISACODYL 5MG | Pharmadel LLC | 3999935b-d8e8-52a6-e063-6294a90aa2a2 | 2026-03-20 | Warnings | M007 |
| Laxative Enteric Coated | BISACODYL 5MG | Grocery Outlet | c820e6a1-fa23-447a-9ee9-50a1bd617adb | 2026-03-19 | Warnings | M007 |
| CITRUCEL | METHYLCELLULOSE | Haleon US Holdings LLC | 9d5f2244-a610-4d45-b6e8-e79bb17a558f | 2026-03-18 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Safeway, Inc. | f178b31d-4843-4b91-a0d5-ab5ade835dc2 | 2026-03-16 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Safeway, Inc. | 12ab9c3c-1f4b-43cd-83ac-b5f80b1aa54c | 2026-03-13 | Warnings | M007 |
| Castor Oil | CASTOR OIL | Old East Main Co. | a1ca668a-3bf9-46a9-8a4f-5cb61547bb81 | 2026-03-12 | Warnings, Adverse reactions | M007 |
| Castor Oil | CASTOR OIL | Vi-Jon, LLC | b29775df-8470-4fe3-bee3-f0490ea6903f | 2026-03-12 | Warnings | M007 |
| Castor Oil | CASTOR OIL | Nice-Pak Products, LLC | cc43d514-ee82-4314-99b2-c64380f98779 | 2026-03-12 | Warnings, Adverse reactions | M007 |
| Fibercon | CALCIUM POLYCARBOPHIL | Foundation Consumer Brands | 7992a4bb-5535-4a1d-867d-a99f7e0c1be7 | 2026-03-12 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Walgreens | cda27a9c-9175-4b07-9c0b-d8d897882965 | 2026-03-12 | Warnings | M007 |
| Magnesium Citrate Saline Laxative - Lemon Flavor | MAGNESIUM CITRATE | Universal Distribution Center LLC | aa02c9af-22b8-4ec2-9e43-fe073f5e617b | 2026-03-11 | Warnings | M007 |
| Magnesium Citrate Saline Laxative - Grape Flavor | MAGNESIUM CITRATE | Universal Distribution Center LLC | 021ebb61-2466-4272-8f7d-b49cafd08754 | 2026-03-11 | Warnings | M007 |
| Magnesium Citrate Saline Laxative - Cherry Flavor | MAGNESIUM CITRATE | Universal Distribution Center LLC | 1f14411b-6833-40e6-b1a5-2b8c5bf709d3 | 2026-03-11 | Warnings | M007 |
| Citroma | MAGNESIUM CITRATE | UpLift Brands, LLC | f83ba007-734d-4910-87cb-02e45285e161 | 2026-03-11 | Warnings, Adverse reactions | M007 |
| Citroma | MAGNESIUM CITRATE | UpLift Brands, LLC | 57e914fa-8fa2-4221-bb5f-534f0ea0aba7 | 2026-03-11 | Warnings, Adverse reactions | M007 |
| Citroma | MAGNESIUM CITRATE | UpLift Brands, LLC | f28a9043-e0ee-4b38-95d9-d3f23d400691 | 2026-03-11 | Warnings, Adverse reactions | M007 |
| Stool Softener | DOCUSATE SODIUM | Amerisource Bergen | 4caf0bcb-c1bf-0ae7-e063-6294a90a344b | 2026-03-10 | Warnings | M007 |
| Stool Softener Laxative | DOCUSATE SODIUM | Walgreens | 92df761b-da68-4ce9-b02a-a5a74fd6620e | 2026-03-10 | Warnings | M007 |
| Fleet | GLYCERIN | C.B. Fleet Company, Inc. | 31778652-e60e-4098-8e90-3e4f56b5800c | 2026-03-06 | Warnings | M007 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308753 | bisacodyl 5 MG Delayed Release Oral Tablet | PSN | 4e0d973f-e6dc-48d9-8df3-1d47c87840f1 | 1 |
| 308753 | bisacodyl 5 MG Delayed Release Oral Tablet | SCD | 4e0d973f-e6dc-48d9-8df3-1d47c87840f1 | 1 |
| 308753 | bisacodyl 5 MG Enteric Coated Oral Tablet | SY | 4e0d973f-e6dc-48d9-8df3-1d47c87840f1 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 0132-0401-25 | 00132040125 | 25 TABLET, COATED in 1 BLISTER PACK (0132-0401-25) | 2024-06-21 | No | No | Current |