docusate sodium oral liquid
Generic: docusate sodium oral liquid
Labeler: kesin pharma corporationDrug Facts
Product Profile
Brand Name
docusate sodium oral liquid
Generic Name
docusate sodium oral liquid
Labeler
kesin pharma corporation
Dosage Form
LIQUID
Routes
Active Ingredients
docusate sodium 100 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
81033-022
Product ID
81033-022_331277b8-8305-d082-e063-6394a90a4dd3
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M007
Listing Expiration
2026-12-31
Marketing Start
2025-04-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81033022
Hyphenated Format
81033-022
Supplemental Identifiers
RxCUI
UNII
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
docusate sodium oral liquid (source: ndc)
Generic Name
docusate sodium oral liquid (source: ndc)
Application Number
M007 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/10mL
Packaging
- 100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "331277b8-8305-d082-e063-6394a90a4dd3", "openfda": {"unii": ["F05Q2T2JA0"], "rxcui": ["1248119"], "spl_set_id": ["331277b8-8304-d082-e063-6394a90a4dd3"], "manufacturer_name": ["Kesin Pharma Corporation"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10)", "package_ndc": "81033-022-50", "marketing_start_date": "20250401"}], "brand_name": "Docusate Sodium Oral Liquid", "product_id": "81033-022_331277b8-8305-d082-e063-6394a90a4dd3", "dosage_form": "LIQUID", "product_ndc": "81033-022", "generic_name": "Docusate Sodium Oral Liquid", "labeler_name": "Kesin Pharma Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Docusate Sodium Oral Liquid", "active_ingredients": [{"name": "DOCUSATE SODIUM", "strength": "100 mg/10mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}