Home NDC 0363-9990 Sennosides
Product NDC 0363-9990
11-digit product format 003639990
Labeler code 0363
Product ID 0363-9990_4652df6c-2990-3528-e063-6394a90ac448
Type HUMAN OTC DRUG
Nonproprietary name Sennosides
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler Walgreens Co
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-29
Substance SENNOSIDES
Active strength 17.2 mg/17.21
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product 0363-9990 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 0363-9990 0363-9990-20 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…
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 SENNOSIDES 17.2 mg/17.21
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3FYP5M0IJX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2169295 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0363-9990-20 Sennosides 200 in 1 BOTTLE CAPSULE, LIQUID FILLED 200 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-9990 SENNOSIDES CAPSULE, LIQUID FILLED [WALGREENS CO] 8 Current NDC, Legacy NDC, 1 package rows 20241218_85a2f7ed-315e-2403-e053-2991aa0abdce.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 17 of 42 · 833 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 0363-9990-20 00363999020 200 CAPSULE, LIQUID FILLED in 1 BOTTLE (0363-9990-20) 2019-05-29 0000-00-00 No No Current