stool softener extra strength
Generic: docusate sodium
Labeler: p & l development, llcDrug Facts
Product Profile
Brand Name
stool softener 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
59726-058
Product ID
59726-058_eb9d2c44-06dd-4804-a2ee-40d39584bc9b
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Marketing Start
2021-06-25
Marketing End
2026-12-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59726058
Hyphenated Format
59726-058
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 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
- 250 CAPSULE, LIQUID FILLED in 1 BOTTLE (59726-058-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "eb9d2c44-06dd-4804-a2ee-40d39584bc9b", "openfda": {"upc": ["0359726258258"], "unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["4e97dd60-96e3-4b51-b614-c62480af1919"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "250 CAPSULE, LIQUID FILLED in 1 BOTTLE (59726-058-25)", "package_ndc": "59726-058-25", "marketing_end_date": "20261231", "marketing_start_date": "20210625"}], "brand_name": "Stool Softener Extra Strength", "product_id": "59726-058_eb9d2c44-06dd-4804-a2ee-40d39584bc9b", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "59726-058", "generic_name": "Docusate Sodium", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "brand_name_suffix": "Extra Strength", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "250 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20210625"}