Package 70000-0526-1

Brand: stool softener plus stimulant laxative

Generic: docusate sodium 50 mg and sennosides 8.6 mg
NDC Package

Package Facts

Identity

Package NDC 70000-0526-1
Digits Only 7000005261
Product NDC 70000-0526
Product ID 70000-0526_b33fb5f0-197e-4a91-b324-af6a97c29f53
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-1)

Marketing

Marketing Status
Marketed Since 2019-10-23
Brand stool softener plus stimulant laxative
Generic docusate sodium 50 mg and sennosides 8.6 mg
Sample Package No

Linked Drug Pages (1)

Stool Softener plus Stimulant Laxative ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b33fb5f0-197e-4a91-b324-af6a97c29f53", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["3fd9ba76-42f8-4ebe-b1bc-f81f08e702ce"], "manufacturer_name": ["CARDINAL HEALTH, 110 DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-1)", "package_ndc": "70000-0526-1", "marketing_start_date": "20191023"}, {"sample": false, "description": "200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-2)", "package_ndc": "70000-0526-2", "marketing_start_date": "20251223"}], "brand_name": "Stool Softener plus Stimulant Laxative", "product_id": "70000-0526_b33fb5f0-197e-4a91-b324-af6a97c29f53", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70000-0526", "generic_name": "Docusate Sodium 50 mg and Sennosides 8.6 mg", "labeler_name": "CARDINAL HEALTH, 110 DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener plus Stimulant Laxative", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191023", "listing_expiration_date": "20271231"}