Package 17856-1248-1
Brand: stimulant laxative plus stool softener
Generic: docusate sodium 50 mg and sennosides 8.6 mgPackage Facts
Identity
Package NDC
17856-1248-1
Digits Only
1785612481
Product NDC
17856-1248
Description
100 POUCH in 1 BOX, UNIT-DOSE (17856-1248-1) / 1 TABLET, FILM COATED in 1 POUCH
Marketing
Marketing Status
Brand
stimulant laxative plus stool softener
Generic
docusate sodium 50 mg and sennosides 8.6 mg
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38930b8a-9e76-2025-e063-6394a90a2478", "openfda": {"unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["4c02fcec-6bb7-4497-96c5-0d809209dd17"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX, UNIT-DOSE (17856-1248-1) / 1 TABLET, FILM COATED in 1 POUCH", "package_ndc": "17856-1248-1", "marketing_start_date": "20240509"}], "brand_name": "Stimulant Laxative Plus Stool Softener", "product_id": "17856-1248_38930b8a-9e76-2025-e063-6394a90a2478", "dosage_form": "TABLET, FILM COATED", "product_ndc": "17856-1248", "generic_name": "Docusate Sodium 50 mg and Sennosides 8.6 mg", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stimulant Laxative Plus Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "50 mg/1"}, {"name": "SENNOSIDES", "strength": "8.6 mg/1"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191022", "listing_expiration_date": "20261231"}