stool softener
Generic: marc glassman
Labeler: marc glassman, inc.Drug Facts
Product Profile
Brand Name
stool softener
Generic Name
marc glassman
Labeler
marc glassman, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
docusate sodium 100 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68998-420
Product ID
68998-420_c80e0e2e-d701-4de9-97cc-a908e9301d59
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2015-04-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68998420
Hyphenated Format
68998-420
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
marc glassman (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE, PLASTIC (68998-420-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c80e0e2e-d701-4de9-97cc-a908e9301d59", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1115005"], "spl_set_id": ["909cd222-d836-416f-aa7d-deb4a0c5a560"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (68998-420-01)", "package_ndc": "68998-420-01", "marketing_start_date": "20190904"}], "brand_name": "Stool Softener", "product_id": "68998-420_c80e0e2e-d701-4de9-97cc-a908e9301d59", "dosage_form": "CAPSULE", "product_ndc": "68998-420", "generic_name": "Marc Glassman", "labeler_name": "Marc Glassman, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stool Softener", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150410", "listing_expiration_date": "20261231"}