stool softener laxative extra strength
Generic: docusate sodium
Labeler: p & l development, llcDrug Facts
Product Profile
Brand Name
stool softener laxative extra strength
Generic Name
docusate sodium
Labeler
p & l development, llc
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
docusate sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
59726-879
Product ID
59726-879_5df65d78-8a3f-42dd-b596-1d1baf4b60c3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2019-11-29
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59726879
Hyphenated Format
59726-879
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 extra strength (source: ndc)
Generic Name
docusate sodium (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-879-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5df65d78-8a3f-42dd-b596-1d1baf4b60c3", "openfda": {"upc": ["0359726285100"], "unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["c1e9863a-c229-4694-b450-6b0e0ad37503"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-879-10)", "package_ndc": "59726-879-10", "marketing_start_date": "20191129"}], "brand_name": "Stool Softener Laxative Extra Strength", "product_id": "59726-879_5df65d78-8a3f-42dd-b596-1d1baf4b60c3", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "59726-879", "generic_name": "Docusate Sodium", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener Laxative", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "250 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20191129", "listing_expiration_date": "20261231"}