stool softener plus stimulant laxative

Generic: docusate sodium 50 mg and sennosides 8.6 mg

Labeler: cardinal health, 110 dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stool softener plus stimulant laxative
Generic Name docusate sodium 50 mg and sennosides 8.6 mg
Labeler cardinal health, 110 dba leader
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

docusate sodium 50 mg/1, sennosides 8.6 mg/1

Manufacturer
CARDINAL HEALTH, 110 DBA LEADER

Identifiers & Regulatory

Product NDC 70000-0526
Product ID 70000-0526_b33fb5f0-197e-4a91-b324-af6a97c29f53
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2027-12-31
Marketing Start 2019-10-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000526
Hyphenated Format 70000-0526

Supplemental Identifiers

RxCUI
998740
UNII
F05Q2T2JA0 3FYP5M0IJX

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name stool softener plus stimulant laxative (source: ndc)
Generic Name docusate sodium 50 mg and sennosides 8.6 mg (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
  • 8.6 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-1)
  • 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-2)
source: ndc

Packages (2)

70000-0526-1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-1) 70000-0526-2 200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70000-0526-2)

Ingredients (2)

docusate sodium (50 mg/1) sennosides (8.6 mg/1)

Linked Drug Pages (1)

Stool Softener plus Stimulant Laxative ndc-match (0.9)

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"}