Stool Softener with 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 with Laxative
Generic name: DOCUSATE SODIUM AND SENNOSIDES
Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
SPL set ID: e24638d3-7738-4185-8ce9-1845d8594cc6
SPL ID: 50ff216f-56d0-4d51-ac30-f08ba4e22cf4
Version: 1
Effective date: 2024-11-04
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:56:19

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		Stool Softener with Laxative	openfda.brand_name
generic name		DOCUSATE SODIUM AND SENNOSIDES	openfda.generic_name
manufacturer name		Bryant Ranch Prepack	openfda.manufacturer_name
ndc	package	71335-2522-4	openfda.package_ndc
ndc	package	71335-2522-3	openfda.package_ndc
ndc	package	71335-2522-5	openfda.package_ndc
ndc	package	71335-2522-7	openfda.package_ndc
ndc	package	71335-2522-6	openfda.package_ndc
ndc	package	71335-2522-1	openfda.package_ndc
ndc	package	71335-2522-9	openfda.package_ndc
ndc	package	71335-2522-8	openfda.package_ndc
ndc	package	71335-2522-2	openfda.package_ndc
ndc	product	71335-2522	openfda.product_ndc
ndc11	package	71335252206	derived:openfda.package_ndc
ndc11	package	71335252205	derived:openfda.package_ndc
ndc11	package	71335252202	derived:openfda.package_ndc
ndc11	package	71335252207	derived:openfda.package_ndc
ndc11	package	71335252208	derived:openfda.package_ndc
ndc11	package	71335252203	derived:openfda.package_ndc
ndc11	package	71335252201	derived:openfda.package_ndc
ndc11	package	71335252204	derived:openfda.package_ndc
ndc11	package	71335252209	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		50ff216f-56d0-4d51-ac30-f08ba4e22cf4	id
spl set id		e24638d3-7738-4185-8ce9-1845d8594cc6	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 directed 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 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. 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.