Home NDC 69842-220 SENNOSIDES
Product NDC 69842-220
11-digit product format 698420220
Labeler code 69842
Product ID 69842-220_28513391-e716-29a1-e063-6394a90a0340
Type HUMAN OTC DRUG
Nonproprietary name SENNOSIDES
Dosage form TABLET, FILM COATED
Route ORAL
Labeler CVS Pharmacy, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2018-07-03
Substance SENNOSIDES
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 SENNOSIDES 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 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 312935 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 69842-220-08 SENNOSIDES 500 in 1 BOTTLE TABLET, FILM COATED 500 5 69842-220-25 SENNOSIDES 250 in 1 BOTTLE TABLET, FILM COATED 250 5 69842-220-50 SENNOSIDES 50 in 1 BOTTLE TABLET, FILM COATED 50 5 69842-220-50 SENNOSIDES 1 in 1 CARTON TABLET, FILM COATED 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-220 SENNOSIDES TABLET, FILM COATED [CVS PHARMACY, INC.] 5 Current NDC, Legacy NDC, 4 package rows 20241208_6dffc3f5-bae0-c436-e053-2991aa0a0f8b.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 Units Marketing start Marketing end Sample Exclude flag Status 69842-220-08 69842022008 500 TABLET, FILM COATED in 1 BOTTLE (69842-220-08) 2021-04-29 0000-00-00 No No Current 69842-220-25 69842022025 250 TABLET, FILM COATED in 1 BOTTLE (69842-220-25) 2018-07-03 0000-00-00 No No Current 69842-220-50 69842022050 1 BOTTLE in 1 CARTON (69842-220-50) / 50 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2018-07-03 0000-00-00 No No Current