stool softener
Generic: docusate sodium
Labeler: hebDrug Facts
Product Profile
Brand Name
stool softener
Generic Name
docusate sodium
Labeler
heb
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
docusate sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-585
Product ID
37808-585_4589467b-a9e7-ec2b-e063-6394a90ade30
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2025-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808585
Hyphenated Format
37808-585
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 (source: ndc)
Generic Name
docusate sodium (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-585-14)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4589467b-a9e7-ec2b-e063-6394a90ade30", "openfda": {"upc": ["0197870178202"], "unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["2f103a88-4cab-d4b9-e063-6394a90ac7fc"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-585-14)", "package_ndc": "37808-585-14", "marketing_start_date": "20250901"}], "brand_name": "Stool Softener", "product_id": "37808-585_4589467b-a9e7-ec2b-e063-6394a90ade30", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "37808-585", "generic_name": "DOCUSATE SODIUM", "labeler_name": "HEB", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "250 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250901", "listing_expiration_date": "20261231"}