Stool Softener Laxative

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: Stool Softener Laxative
Generic name: DOCUSATE SODIUM
Manufacturer: CVS Pharmacy
Product type: HUMAN OTC DRUG
SPL set ID: f77c65b0-3e13-48ce-a2d9-36a9eba1851f
SPL ID: 45f92987-a003-4258-a2ca-e62060a17887
Version: 6
Effective date: 2024-03-07
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:03:50

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 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Stool Softener Laxative	openfda.brand_name
generic name		DOCUSATE SODIUM	openfda.generic_name
manufacturer name		CVS Pharmacy	openfda.manufacturer_name
ndc	package	69842-782-25	openfda.package_ndc
ndc	package	69842-782-75	openfda.package_ndc
ndc	package	69842-782-10	openfda.package_ndc
ndc	package	69842-782-30	openfda.package_ndc
ndc	package	69842-782-40	openfda.package_ndc
ndc	product	69842-782	openfda.product_ndc
ndc11	package	69842078275	derived:openfda.package_ndc
ndc11	package	69842078240	derived:openfda.package_ndc
ndc11	package	69842078230	derived:openfda.package_ndc
ndc11	package	69842078210	derived:openfda.package_ndc
ndc11	package	69842078225	derived:openfda.package_ndc
rxcui		1115005	openfda.rxcui
spl id		45f92987-a003-4258-a2ca-e62060a17887	id
spl set id		f77c65b0-3e13-48ce-a2d9-36a9eba1851f	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, unless told to do so by a doctor. Ask a doctor before use if you have stomach pain nausea vomiting a sudden change in bowel habits that lasts over 2 weeks Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition. you need to use a laxative for more than 1 week 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 (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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