Home NDC 81005-102 Senna-S
Product NDC 81005-102
11-digit product format 810050102
Labeler code 81005
Product ID 81005-102_575f958c-2cca-d730-e063-6294a90ac5ac
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium 50 mg Sennosides 8.6 mg
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Aarkish Pharmaceuticals NJ Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-01
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 Senna-S
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.
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 Marketing start Sample Exclude flag Status 81005-102-10 81005010210 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81005-102-10) 2026-07-01 No No Current 81005-102-30 81005010230 300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81005-102-30) 2026-07-01 No No Current