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: Ulai Health LLC
Product type: HUMAN OTC DRUG
SPL set ID: c0e27b02-8ef2-4239-8f8c-790f7d978dc0
SPL ID: 2c270be1-981f-3019-e063-6394a90a098f
Version: 3
Effective date: 2025-01-12
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:07

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		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		Ulai Health LLC	openfda.manufacturer_name
ndc	package	73057-378-07	openfda.package_ndc
ndc	package	73057-378-11	openfda.package_ndc
ndc	package	73057-378-08	openfda.package_ndc
ndc	product	73057-378	openfda.product_ndc
ndc11	package	73057037807	derived:openfda.package_ndc
ndc11	package	73057037811	derived:openfda.package_ndc
ndc11	package	73057037808	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		2c270be1-981f-3019-e063-6394a90a098f	id
spl set id		c0e27b02-8ef2-4239-8f8c-790f7d978dc0	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 if you are taking mineral oil, unless directed by a doctor laxative products for longer than 1 week 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 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 (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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