Home NDC 70677-1091 Foster and Thrive Gentle Laxative
Product NDC 70677-1091
11-digit product format 706771091
Labeler code 70677
Product ID 70677-1091_f8e211ca-4ee0-4561-b8aa-d808511dc6c7
Type HUMAN OTC DRUG
Nonproprietary name Bisacodyl
Dosage form SUPPOSITORY
Route RECTAL
Labeler Strategic Sourcing Services LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-27
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 Foster and Thrive 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 70677-1091-1 Foster and Thrive Gentle Laxative 2 in 1 CARTON SUPPOSITORY 2 3 70677-1091-1 Foster and Thrive Gentle Laxative 40 mg in 1 BLISTER PACK SUPPOSITORY 40 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70677-1091 FOSTER AND THRIVE GENTLE LAXATIVE (BISACODYL ) SUPPOSITORY [STRATEGIC SOURCING SERVICES LLC] 3 Current NDC, 2 package rows 20241220_d03c2c42-d9d9-4b4b-a6ae-31d99425a228.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 Sample Exclude flag Status 70677-1091-1 70677109101 2 BLISTER PACK in 1 CARTON (70677-1091-1) / 40 mg in 1 BLISTER PACK 2 blister pack 2024-12-18 No No Current