Stimulant Laxative

Product NDC
51316-327
11-digit product format
513160327
Labeler code
51316
Product ID
51316-327_92413aec-f608-4a9e-8b6a-3c4df3250277
Type
HUMAN OTC DRUG
Nonproprietary name
Bisacodyl
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-07-07
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
2027-12-31
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
Stimulant Laxative
Brand name suffix
Gentle
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BISACODYL5 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
10X0709Y6IInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
308753Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
cb6d0135-92c6-4078-954c-b7549302145fAvailable on FDA.report

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stimulant Laxative GentleBISACODYLCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDcb6d0135-92c6-4078-954c-b7549302145f2026-08-24WarningsExact identifier
ndc (product): 51316-327

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
51316-327-03513160327031 BLISTER PACK in 1 CARTON (51316-327-03) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK1 blister pack2026-07-07NoNoCurrent
51316-327-15513160327152 BLISTER PACK in 1 CARTON (51316-327-15) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK2 blister pack2026-07-23NoNoCurrent
51316-327-33513160327337 BLISTER PACK in 1 CARTON (51316-327-33) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK7 blister pack2026-08-21NoNoCurrent
51316-327-56513160327561 BLISTER PACK in 1 CARTON (51316-327-56) / 25 TABLET, DELAYED RELEASE in 1 BLISTER PACK1 blister pack2026-07-07NoNoCurrent