Home NDC 70000-0526 Stool Softener plus Stimulant Laxative
Product NDC 70000-0526
11-digit product format 700000526
Labeler code 70000
Product ID 70000-0526_b33fb5f0-197e-4a91-b324-af6a97c29f53
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium 50 mg and Sennosides 8.6 mg
Dosage form TABLET, FILM COATED
Route ORAL
Labeler CARDINAL HEALTH, 110 DBA LEADER
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-10-23
Substance SENNOSIDES; DOCUSATE SODIUM
Active strength 8.6; 50 mg/1; mg/1
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 Stool Softener plus Stimulant Laxative
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SENNOSIDES 8.6 mg/1 DOCUSATE SODIUM 50 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3FYP5M0IJX Internal UNII lookup F05Q2T2JA0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998740 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0526-1 Stool Softener plus Stimulant Laxative 100 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 100 5 70000-0526-2 Stool Softener plus Stimulant Laxative 200 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 200 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0526 STOOL SOFTENER PLUS STIMULANT LAXATIVE (DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG) TABLET, FILM COATED [CARDINAL HEALTH, 110 DBA LEADER] 3 Current NDC, Legacy NDC, 2 package rows 20241226_3fd9ba76-42f8-4ebe-b1bc-f81f08e702ce.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 · 829 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 70000-0526-1 70000052601 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-1) 2019-10-23 0000-00-00 No No Current 70000-0526-2 70000052602 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-2) 2025-12-23 No No Current