stool softener
Generic: docusate sodium
Labeler: h e bDrug Facts
Product Profile
Brand Name
stool softener
Generic Name
docusate sodium
Labeler
h e b
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
docusate sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37808-879
Product ID
37808-879_ad646c69-031a-4194-a32c-df17be7e08e8
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2021-03-26
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37808879
Hyphenated Format
37808-879
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 (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 (37808-879-14)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ad646c69-031a-4194-a32c-df17be7e08e8", "openfda": {"upc": ["0041220541706"], "unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["1dd2be7e-bdca-4e43-b853-3ed10b636632"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "140 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-879-14)", "package_ndc": "37808-879-14", "marketing_start_date": "20210326"}], "brand_name": "Stool Softener", "product_id": "37808-879_ad646c69-031a-4194-a32c-df17be7e08e8", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "37808-879", "generic_name": "Docusate Sodium", "labeler_name": "H E B", "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": "20210326", "listing_expiration_date": "20261231"}