Senna

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
Generic name: SENNOSIDES
Manufacturer: Patrin Pharma, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: a9f1ef8d-8700-481f-a709-972bb9d27153
SPL ID: b42865b6-223b-461b-aabd-ca548a0339fa
Version: 1
Effective date: 2024-05-30
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 05:38:15

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 · 24 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M007	openfda.application_number
brand name		Senna	openfda.brand_name
brand name		Senna UD	openfda.brand_name
generic name		SENNOSIDES	openfda.generic_name
manufacturer name		Patrin Pharma, Inc.	openfda.manufacturer_name
ndc	package	39328-220-50	openfda.package_ndc
ndc	package	39328-220-15	openfda.package_ndc
ndc	package	39328-020-08	openfda.package_ndc
ndc	package	39328-120-05	openfda.package_ndc
ndc	package	39328-120-50	openfda.package_ndc
ndc	package	39328-120-99	openfda.package_ndc
ndc	product	39328-120	openfda.product_ndc
ndc	product	39328-220	openfda.product_ndc
ndc	product	39328-020	openfda.product_ndc
ndc11	package	39328002008	derived:openfda.package_ndc
ndc11	package	39328012005	derived:openfda.package_ndc
ndc11	package	39328012099	derived:openfda.package_ndc
ndc11	package	39328022050	derived:openfda.package_ndc
ndc11	package	39328012050	derived:openfda.package_ndc
ndc11	package	39328022015	derived:openfda.package_ndc
rxcui		702311	openfda.rxcui
spl id		b42865b6-223b-461b-aabd-ca548a0339fa	id
spl set id		a9f1ef8d-8700-481f-a709-972bb9d27153	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 one week unless directed by a doctor. Ask a doctor before use if you have stomach pain, nausea or vomiting notice a change in bowel habits that last over two weeks are pregnant or breast feeding Stop use and ask a doctor if you have rectal bleeding or failure to have a bowel movement after use. Keep out of reach of children. In case of accidental 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.