Package 79481-0304-1

Brand: stool softener plus stimulant laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 79481-0304-1
Digits Only 7948103041
Product NDC 79481-0304
Description

100 TABLET, FILM COATED in 1 BOTTLE (79481-0304-1)

Marketing

Marketing Status
Marketed Since 2025-03-01
Brand stool softener plus stimulant laxative
Generic docusate sodium and sennosides
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3118c301-06ff-fd57-e063-6294a90a916f", "openfda": {"upc": ["0713733507592"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["261a88d6-87d2-7544-e063-6294a90a2e94"], "manufacturer_name": ["Meijer, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (79481-0304-1)", "package_ndc": "79481-0304-1", "marketing_start_date": "20250301"}], "brand_name": "Stool Softener plus Stimulant Laxative", "product_id": "79481-0304_3118c301-06ff-fd57-e063-6294a90a916f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "79481-0304", "generic_name": "Docusate Sodium and Sennosides", "labeler_name": "Meijer, Inc.", "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": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}