Home NDC 41250-665 Meijer Gentle Laxative
Product NDC 41250-665
11-digit product format 412500665
Labeler code 41250
Product ID 41250-665_a34ed0dd-d1c1-480e-9f9c-f703d0da0230
Type HUMAN OTC DRUG
Nonproprietary name Bisacodyl
Dosage form SUPPOSITORY
Route RECTAL
Labeler Meijer Distribution Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-02-26
Substance BISACODYL
Active strength 10 mg/2000mg
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 Meijer Gentle Laxative
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISACODYL 10 mg/2000mg
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 41250-665-04 Meijer Gentle Laxative 40 mg in 1 BLISTER PACK SUPPOSITORY 40 6 41250-665-04 Meijer Gentle Laxative 1 in 1 CARTON SUPPOSITORY 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41250-665 MEIJER GENTLE LAXATIVE (BISACODYL ) SUPPOSITORY [MEIJER DISTRIBUTION INC.] 6 Current NDC, Legacy NDC, 2 package rows 20241220_b49786a1-f0b9-45ae-b8f6-683489c54e76.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 17 of 42 · 833 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 41250-665-04 41250066504 1 BLISTER PACK in 1 CARTON (41250-665-04) / 40 mg in 1 BLISTER PACK 1 blister pack 2020-02-26 0000-00-00 No No Current