stool softener laxative

Generic: docusate sodium and sennosides

Labeler: p & l development, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name stool softener laxative
Generic Name docusate sodium and sennosides
Labeler p & l development, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
P & L Development, LLC

Identifiers & Regulatory

Product NDC 59726-778
Product ID 59726-778_7fc75843-4bdd-4d57-a2f4-4d82171553fc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Marketing Start 2021-03-26
Marketing End 2027-03-27

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59726778
Hyphenated Format 59726-778

Supplemental Identifiers

RxCUI
998740
UPC
0359726885102
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 laxative (source: ndc)
Generic Name docusate sodium and sennosides (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 in 1 BOTTLE (59726-778-10)
source: ndc

Packages (1)

59726-778-10 100 TABLET in 1 BOTTLE (59726-778-10)

Ingredients (2)

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

Linked Drug Pages (1)

Stool Softener Laxative ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7fc75843-4bdd-4d57-a2f4-4d82171553fc", "openfda": {"upc": ["0359726885102"], "unii": ["F05Q2T2JA0", "3FYP5M0IJX"], "rxcui": ["998740"], "spl_set_id": ["84ee167d-18f2-4381-ba9e-8500869e6ef9"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59726-778-10)", "package_ndc": "59726-778-10", "marketing_end_date": "20270327", "marketing_start_date": "20210326"}], "brand_name": "Stool Softener Laxative", "product_id": "59726-778_7fc75843-4bdd-4d57-a2f4-4d82171553fc", "dosage_form": "TABLET", "product_ndc": "59726-778", "generic_name": "docusate sodium and sennosides", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener 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_end_date": "20270327", "marketing_start_date": "20210326"}