Home NDC 41415-121 Publix Women
Product NDC 41415-121
11-digit product format 414150121
Labeler code 41415
Product ID 41415-121_423691f9-9ab1-fad0-e063-6394a90a8d1b
Type HUMAN OTC DRUG
Nonproprietary name Bisacodyl
Dosage form TABLET
Route ORAL
Labeler PUBLIX SUPER MARKETS, INC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-22
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 Publix Women
Brand name suffix Laxative
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BISACODYL 5 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 308753 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 41415-121-30 Publix WomenLaxative 2 in 1 CARTON TABLET 2 7 41415-121-30 Publix WomenLaxative 15 in 1 BLISTER PACK TABLET 15 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41415-121 PUBLIX WOMEN LAXATIVE (BISACODYL) TABLET [PUBLIX SUPER MARKETS, INC] 6 Current NDC, Legacy NDC, 2 package rows 20241030_03eeca55-f239-4a01-a900-c1943f27a834.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 14 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 41415-121-30 41415012130 2 BLISTER PACK in 1 CARTON (41415-121-30) / 15 TABLET in 1 BLISTER PACK 2 blister pack 2019-05-22 0000-00-00 No No Current