Home NDC 76420-918 Sennosides and Docusate Sodium
Product NDC 76420-918
11-digit product format 764200918
Labeler code 76420
Product ID 76420-918_2d9d8f71-cc36-459a-e063-6394a90acf8e
Type HUMAN OTC DRUG
Nonproprietary name Sennosides, Docusate Sodium
Dosage form TABLET
Route ORAL
Labeler Asclemed USA, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-08-01
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 Sennosides and Docusate Sodium
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76420-918-01 Sennosides and Docusate Sodium 100 in 1 BOTTLE TABLET 100 1 76420-918-30 Sennosides and Docusate Sodium 30 in 1 BOTTLE TABLET 30 1 76420-918-60 Sennosides and Docusate Sodium 60 in 1 BOTTLE TABLET 60 1 76420-918-90 Sennosides and Docusate Sodium 90 in 1 BOTTLE TABLET 90 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76420-918 SENNOSIDES AND DOCUSATE SODIUM (SENNOSIDES, DOCUSATE SODIUM) TABLET [ASCLEMED USA, INC.] 1 Current NDC, 4 package rows 20250212_2db546de-20dc-4697-aff2-12471f073b1d.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 · 833 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 76420-918-01 76420091801 100 TABLET in 1 BOTTLE (76420-918-01) 100 tablet 2025-02-08 No No Current 76420-918-30 76420091830 30 TABLET in 1 BOTTLE (76420-918-30) 30 tablet 2025-02-08 No No Current 76420-918-60 76420091860 60 TABLET in 1 BOTTLE (76420-918-60) 60 tablet 2025-02-08 No No Current 76420-918-90 76420091890 90 TABLET in 1 BOTTLE (76420-918-90) 90 tablet 2025-02-08 No No Current