Home NDC 81033-022 Docusate Sodium Oral Liquid
Product NDC 81033-022
11-digit product format 810330022
Labeler code 81033
Product ID 81033-022_331277b8-8305-d082-e063-6394a90a4dd3
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium Oral Liquid
Dosage form LIQUID
Route ORAL
Labeler Kesin Pharma Corporation
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-01
Substance DOCUSATE SODIUM
Active strength 100 mg/10mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings Do not use for more than 1 week unless directed by a doctor if you are currently taking mineral oil, unless directed by a doctor Ask a doctor before use if you have stomach pain nausea vomiting noticed a sudden change in bowel habits that persists over a period of 2 weeks Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use of a laxative. These could be signs of a serious condition. a skin rash occurs you experience throat irritation
Additional Listing Data#
Finished product Yes
Brand name base Docusate Sodium Oral Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DOCUSATE SODIUM 100 mg/10mL
Harmonized Identifiers# Field, Values table Field Values Unii F05Q2T2JA0 Rxcui 1248119
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81033-022-10 Docusate Sodium Oral Liquid 10 mL in 1 CUP, UNIT-DOSE LIQUID 10 1 81033-022-50 Docusate Sodium Oral Liquid 100 in 1 CASE LIQUID 100 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81033-022 DOCUSATE SODIUM ORAL LIQUID LIQUID [KESIN PHARMA CORPORATION] 1 Current NDC, 2 package rows 20250427_331277b8-8304-d082-e063-6394a90a4dd3.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81033-022-10 81033002210 10 mL in 1 CUP, UNIT-DOSE 10 ml Historical 81033-022-50 81033002250 100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10) 2025-04-01 No No Current