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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Docusate Sodium Oral LiquidDOCUSATE SODIUM ORAL LIQUIDKesin Pharma Corporation331277b8-8304-d082-e063-6394a90a4dd32025-04-18WarningsExact identifier

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
IngredientStrength
DOCUSATE SODIUM100 mg/10mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF05Q2T2JA0
Rxcui1248119

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81033-022-10Docusate Sodium Oral Liquid10 mL in 1 CUP, UNIT-DOSELIQUID101
81033-022-50Docusate Sodium Oral Liquid100 in 1 CASELIQUID1001

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
81033-022-10ML - Milliliter81033-022592e48d2-2f24-4f2f-b824-d15fadcaf4be12025-05-14
81033-022-50ML - Milliliter81033-0222088ee40-f975-4ca9-b2a3-65a3d197142812025-05-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81033-022DOCUSATE SODIUM ORAL LIQUID LIQUID [KESIN PHARMA CORPORATION]1Current NDC, 2 package rows20250427_331277b8-8304-d082-e063-6394a90a4dd3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1248119docusate sodium 50 MG in 5 mL Oral SuspensionPSN331277b8-8304-d082-e063-6394a90a4dd31
1248119docusate sodium 10 MG/ML Oral SuspensionSCD331277b8-8304-d082-e063-6394a90a4dd31
1248119docusate sodium 100 MG per 10 ML Oral SuspensionSY331277b8-8304-d082-e063-6394a90a4dd31
1248119docusate sodium 150 MG per 15 ML Oral SuspensionSY331277b8-8304-d082-e063-6394a90a4dd31
1248119docusate sodium 50 MG per 5 ML Oral SuspensionSY331277b8-8304-d082-e063-6394a90a4dd31
1248119DOSS Sodium 10 MG/ML Oral SuspensionSY331277b8-8304-d082-e063-6394a90a4dd31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
81033-022-108103300221010 mL in 1 CUP, UNIT-DOSE10 mlHistorical
81033-022-5081033002250100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10) 2025-04-01NoNoCurrent