DOCUZEN

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: DOCUZEN
Generic name: SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG
Manufacturer: Village Pharma
Product type: HUMAN OTC DRUG
SPL set ID: 29102014-9b0e-4899-958d-83111f94a612
SPL ID: bf899923-8769-4738-88ea-b1a07997b959
Version: 3
Effective date: 2025-06-01
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:44:45

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		DOCUZEN	openfda.brand_name
generic name		SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG	openfda.generic_name
manufacturer name		Village Pharma	openfda.manufacturer_name
ndc	package	71574-700-60	openfda.package_ndc
ndc	product	71574-700	openfda.product_ndc
ndc11	package	71574070060	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		bf899923-8769-4738-88ea-b1a07997b959	id
spl set id		29102014-9b0e-4899-958d-83111f94a612	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 taking mineral oils, unlesss directed by a doctor Ask a doctor before use if you have • stomach pain • nausea • vomiting • noticed a sudden change in bowel habits that continues over a period of 2 weeks Stop use and ask a doctor if • you have rectal bleeding • you fail to have a bowel movement after the use of a laxative. These may indicate a serious condition. If pregnant or breast feeding, ask a healthcare professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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