Docu 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: Docu Liquid
Generic name: DOCUSATE SODIUM
Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN OTC DRUG
SPL set ID: f4ed0721-3be9-4108-a6c9-dbbe115249e9
SPL ID: 3b3f3045-55db-5ed5-e063-6294a90aab75
Version: 3
Effective date: 2025-07-31
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:55:07

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M	openfda.application_number
brand name		Docu Liquid	openfda.brand_name
generic name		DOCUSATE SODIUM	openfda.generic_name
manufacturer name		ATLANTIC BIOLOGICALS CORP.	openfda.manufacturer_name
ndc	package	17856-0771-1	openfda.package_ndc
ndc	package	17856-0771-2	openfda.package_ndc
ndc	product	17856-0771	openfda.product_ndc
ndc11	package	17856077101	derived:openfda.package_ndc
ndc11	package	17856077102	derived:openfda.package_ndc
rxcui		1248119	openfda.rxcui
spl id		3b3f3045-55db-5ed5-e063-6294a90aab75	id
spl set id		f4ed0721-3be9-4108-a6c9-dbbe115249e9	set_id
unii		F05Q2T2JA0	openfda.unii

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 if you are presently taking mineral oil when abdominal pain, nausea, or vomiting are present for longer than one week Ask a doctor before use if you have noticed a sudden change in bowel habits that lasts over two weeks. Ask a doctor or pharmacist before use if you are taking any other drug. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work. Stop use and ask a doctor if you have rectal bleeding you fail to have a bowel movement after use of this product These may indicate a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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