stool softener
Generic: docusate sodium
Labeler: bi-martDrug Facts
Product Profile
Brand Name
stool softener
Generic Name
docusate sodium
Labeler
bi-mart
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
docusate sodium 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
37835-223
Product ID
37835-223_32847ea7-2479-c06d-e063-6294a90af3b3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2025-03-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
37835223
Hyphenated Format
37835-223
Supplemental Identifiers
RxCUI
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
- 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (37835-223-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32847ea7-2479-c06d-e063-6294a90af3b3", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1245468"], "spl_set_id": ["6589d373-0696-44c2-a9d4-a76e45526c5a"], "manufacturer_name": ["Bi-Mart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, LIQUID FILLED in 1 BOTTLE (37835-223-01)", "package_ndc": "37835-223-01", "marketing_start_date": "20250301"}], "brand_name": "STOOL SOFTENER", "product_id": "37835-223_32847ea7-2479-c06d-e063-6294a90af3b3", "dosage_form": "CAPSULE, LIQUID FILLED", "product_ndc": "37835-223", "generic_name": "DOCUSATE SODIUM", "labeler_name": "Bi-Mart", "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": "20250301", "listing_expiration_date": "20261231"}