Home NDC 57631-016 Sennosides
Product NDC 57631-016
11-digit product format 576310016
Labeler code 57631
Product ID 57631-016_403d9199-afba-4f1b-e063-6294a90aa7df
Type HUMAN OTC DRUG
Nonproprietary name Sennosides
Dosage form TABLET
Route ORAL
Labeler InvaTech Pharma Solutions LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-01-13
Substance SENNA ALATA LEAF
Active strength 8.6 mg/1
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 Sennosides
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SENNA ALATA LEAF 8.6 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4BXR6YZN92 Internal UNII 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 57631-016-00 Sennosides 50000 in 1 BOX TABLET 50000 4
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 57631-016-00 57631001600 50000 TABLET in 1 BOX (57631-016-00) 50000 tablet 2021-01-13 No No Current