Stool Softener Plus Stimulant 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 Plus Stimulant Laxative
Generic name: DOCUSATE SODIUM AND SENNOSIDES
Manufacturer: CVS Pharmacy
Product type: HUMAN OTC DRUG
SPL set ID: 1ed3a4d3-629c-4d70-ac03-d0db9f77a9c8
SPL ID: 02721327-2031-433b-8a5e-5c5b526b577d
Version: 10
Effective date: 2025-11-06
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:38:05

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Stool Softener Plus Stimulant Laxative	openfda.brand_name
generic name		DOCUSATE SODIUM AND SENNOSIDES	openfda.generic_name
manufacturer name		CVS Pharmacy	openfda.manufacturer_name
ndc	package	69842-887-40	openfda.package_ndc
ndc	package	69842-887-10	openfda.package_ndc
ndc	package	69842-887-25	openfda.package_ndc
ndc	product	69842-887	openfda.product_ndc
ndc11	package	69842088740	derived:openfda.package_ndc
ndc11	package	69842088725	derived:openfda.package_ndc
ndc11	package	69842088710	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		02721327-2031-433b-8a5e-5c5b526b577d	id
spl set id		1ed3a4d3-629c-4d70-ac03-d0db9f77a9c8	set_id
unii		3FYP5M0IJX	openfda.unii
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 laxative products for longer than 1 week unless directed by a doctor 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 noticed a sudden change in bowel habits that lasts over a period of 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 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.