Senna Syrup

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 Syrup
Generic name: SENNOSIDES
Manufacturer: Everpharm LLC
Product type: HUMAN OTC DRUG
SPL set ID: 0ea9f2b5-4533-4b71-b019-10ecb3c06459
SPL ID: 2bd9c5d2-3651-de01-e063-6294a90a5e37
Version: 1
Effective date: 2025-01-16
Source export date: 2026-11-06
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:51:01

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Senna Syrup	openfda.brand_name
generic name		SENNOSIDES	openfda.generic_name
manufacturer name		Everpharm LLC	openfda.manufacturer_name
ndc	package	84415-021-01	openfda.package_ndc
ndc	product	84415-021	openfda.product_ndc
ndc11	package	84415002101	derived:openfda.package_ndc
rxcui		702311	openfda.rxcui
spl id		2bd9c5d2-3651-de01-e063-6294a90a5e37	id
spl set id		0ea9f2b5-4533-4b71-b019-10ecb3c06459	set_id
unii		3FYP5M0IJX	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. Ask a doctor before use if you have stomach pain, nausea, or vomiting noticed a change in bowel habits that lasts over two weeks Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use of laxative. These may indicate a serious condition.

Reported adverse events (FAERS/openFDA)#

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