Home NDC 70000-0610-03 NDC 70000-0610-03 - Sennosides This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 70000-0610
Requested NDC 70000-0610-03
Package NDCs from labels 70000-0610-1, 70000-0610-3, 70000-0610-2, 70000-0610-03
Manufacturer LEADER/ Cardinal Health 110, Inc.
Effective date 2026-08-04
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type 1122W - Cardinal LEADER/ Cardinal Health 110, Inc. 2026-08-04 HUMAN OTC DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70000-0610-1 Sennosides 50 in 1 BOTTLE TABLET, FILM COATED 50 3 70000-0610-2 Sennosides 1 in 1 CARTON TABLET, FILM COATED 1 3 70000-0610-2 Sennosides 100 in 1 BOTTLE TABLET, FILM COATED 100 3 70000-0610-3 Sennosides 250 in 1 BOTTLE TABLET, FILM COATED 250 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70000-0610 SENNOSIDES TABLET, FILM COATED [LEADER/ CARDINAL HEALTH 110, INC.] 3 Current NDC, Legacy NDC, 4 package rows 20250213_e3c7ece8-82f3-cd0c-e053-2995a90ad800.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 1 of 56 · 1,112 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.