Docusate Sodium Liquid

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Docusate Sodium Liquid
Generic name
DOCUSATE SODIUM
Manufacturer
LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION
Product type
HUMAN OTC DRUG
SPL set ID
2d8bdd3e-f6e6-43f5-b3b0-e5a882cae41c
SPL ID
4745fe35-8aba-b427-e063-6394a90ab073
Version
9
Effective date
2025-12-31
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:34:59
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use when abdominal pain, nausea, or vomiting are present unless directed by a doctor for more than one week unless directed by a doctor Ask a doctore before use if you are taking mineral oil have noticed a sudden change in bowel habits that last more than two weeks Stop use and ask doctor if you have no bowel movements within 3 days you have rectal bleeding these could be signs of a serious condition a skin rash occurs you experience throat irritation

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.