Package 41163-829-10

Brand: stool softener plus stimulant laxative

Generic: docusate sodium and sennosides
NDC Package

Package Facts

Identity

Package NDC 41163-829-10
Digits Only 4116382910
Product NDC 41163-829
Description

100 TABLET in 1 BOTTLE, PLASTIC (41163-829-10)

Marketing

Marketing Status
Marketed Since 2018-12-31
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": "d1718be3-786c-4808-b125-3280248b868c", "openfda": {"upc": ["0041163256958"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["50ca1ce2-885f-4b71-a5fb-90c2cf508ce6"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (41163-829-10)", "package_ndc": "41163-829-10", "marketing_start_date": "20181231"}], "brand_name": "Stool Softener Plus Stimulant Laxative", "product_id": "41163-829_d1718be3-786c-4808-b125-3280248b868c", "dosage_form": "TABLET", "product_ndc": "41163-829", "generic_name": "docusate sodium and sennosides", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "brand_name_suffix": "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": "20181231", "listing_expiration_date": "20261231"}