stool softener docusate sodium
Generic: docusate sodium
Labeler: magno-humphries, inc.Drug Facts
Product Profile
Brand Name
stool softener docusate sodium
Generic Name
docusate sodium
Labeler
magno-humphries, inc.
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
docusate sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
54257-902
Product ID
54257-902_08bf70ec-89c9-36e5-e063-6294a90a6772
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2020-01-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
54257902
Hyphenated Format
54257-902
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 docusate sodium (source: ndc)
Generic Name
docusate sodium (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 CAPSULE, GELATIN COATED in 1 BOTTLE (54257-902-02)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "08bf70ec-89c9-36e5-e063-6294a90a6772", "openfda": {"upc": ["0043292556039"], "unii": ["F05Q2T2JA0"], "rxcui": ["1115005"], "spl_set_id": ["9d22d642-8aed-d17e-e053-2995a90ae182"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (54257-902-02)", "package_ndc": "54257-902-02", "marketing_start_date": "20200124"}], "brand_name": "Stool Softener Docusate Sodium", "product_id": "54257-902_08bf70ec-89c9-36e5-e063-6294a90a6772", "dosage_form": "CAPSULE, GELATIN COATED", "product_ndc": "54257-902", "generic_name": "DOCUSATE SODIUM", "labeler_name": "Magno-Humphries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener Docusate Sodium", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200124", "listing_expiration_date": "20261231"}