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: SENNA
Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN OTC DRUG
SPL set ID: 8b7cc0d5-029b-43f7-a050-8771e7db4551
SPL ID: 3b3f526b-e72b-4c6d-e063-6394a90a62e3
Version: 4
Effective date: 2025-07-31
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:37:40

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M	openfda.application_number
brand name		SENNA	openfda.brand_name
generic name		SENNA	openfda.generic_name
manufacturer name		ATLANTIC BIOLOGICALS CORP.	openfda.manufacturer_name
ndc	package	17856-8237-1	openfda.package_ndc
ndc	package	17856-8237-5	openfda.package_ndc
ndc	package	17856-8237-8	openfda.package_ndc
ndc	package	17856-8237-7	openfda.package_ndc
ndc	package	17856-8237-6	openfda.package_ndc
ndc	package	17856-8237-3	openfda.package_ndc
ndc	package	17856-8237-4	openfda.package_ndc
ndc	product	17856-8237	openfda.product_ndc
ndc11	package	17856823707	derived:openfda.package_ndc
ndc11	package	17856823704	derived:openfda.package_ndc
ndc11	package	17856823705	derived:openfda.package_ndc
ndc11	package	17856823701	derived:openfda.package_ndc
ndc11	package	17856823706	derived:openfda.package_ndc
ndc11	package	17856823703	derived:openfda.package_ndc
ndc11	package	17856823708	derived:openfda.package_ndc
rxcui		702311	openfda.rxcui
spl id		3b3f526b-e72b-4c6d-e063-6394a90a62e3	id
spl set id		8b7cc0d5-029b-43f7-a050-8771e7db4551	set_id
unii		1B5FPI42EN	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 or pharmacist before use if you have • stomach pain • nausea • vomiting • notice a sudden change in bowel movement that continues over a period of 2 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 If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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