Senna-S

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: Senna-S
Generic name: SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG
Manufacturer: Proficient Rx LP
Product type: HUMAN OTC DRUG
SPL set ID: 8678a3ee-0e2c-4c95-ad2e-83aa601f3238
SPL ID: 4fa397fd-b64f-4219-962e-8d3ba9261778
Version: 2
Effective date: 2024-10-01
Source export date: 2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:18:11

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 · 22 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Senna-S	openfda.brand_name
generic name		SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG	openfda.generic_name
manufacturer name		Proficient Rx LP	openfda.manufacturer_name
ndc	package	71205-970-11	openfda.package_ndc
ndc	package	71205-970-00	openfda.package_ndc
ndc	package	71205-970-30	openfda.package_ndc
ndc	package	71205-970-90	openfda.package_ndc
ndc	package	71205-970-55	openfda.package_ndc
ndc	package	71205-970-60	openfda.package_ndc
ndc	product	71205-970	openfda.product_ndc
ndc11	package	71205097000	derived:openfda.package_ndc
ndc11	package	71205097011	derived:openfda.package_ndc
ndc11	package	71205097055	derived:openfda.package_ndc
ndc11	package	71205097090	derived:openfda.package_ndc
ndc11	package	71205097060	derived:openfda.package_ndc
ndc11	package	71205097030	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		4fa397fd-b64f-4219-962e-8d3ba9261778	id
spl set id		8678a3ee-0e2c-4c95-ad2e-83aa601f3238	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 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 continues 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 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.