SENNA-PLUS

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-PLUS
Generic name: SENNOSIDES AND DOCUSATE SODIUM
Manufacturer: Bryant Ranch Prepack
Product type: HUMAN OTC DRUG
SPL set ID: 7f8396e7-07f0-4c9c-be8a-9dc00139cb83
SPL ID: efcc90d6-8e49-47f4-a370-4bc1156cf742
Version: 3
Effective date: 2024-04-04
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 06:18:14

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 · 28 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		SENNA-PLUS	openfda.brand_name
generic name		SENNOSIDES AND DOCUSATE SODIUM	openfda.generic_name
manufacturer name		Bryant Ranch Prepack	openfda.manufacturer_name
ndc	package	71335-1674-1	openfda.package_ndc
ndc	package	71335-1674-8	openfda.package_ndc
ndc	package	71335-1674-2	openfda.package_ndc
ndc	package	71335-1674-9	openfda.package_ndc
ndc	package	71335-1674-7	openfda.package_ndc
ndc	package	71335-1674-4	openfda.package_ndc
ndc	package	71335-1674-3	openfda.package_ndc
ndc	package	71335-1674-5	openfda.package_ndc
ndc	package	71335-1674-6	openfda.package_ndc
ndc	product	71335-1674	openfda.product_ndc
ndc11	package	71335167403	derived:openfda.package_ndc
ndc11	package	71335167409	derived:openfda.package_ndc
ndc11	package	71335167407	derived:openfda.package_ndc
ndc11	package	71335167406	derived:openfda.package_ndc
ndc11	package	71335167401	derived:openfda.package_ndc
ndc11	package	71335167408	derived:openfda.package_ndc
ndc11	package	71335167405	derived:openfda.package_ndc
ndc11	package	71335167402	derived:openfda.package_ndc
ndc11	package	71335167404	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		efcc90d6-8e49-47f4-a370-4bc1156cf742	id
spl set id		7f8396e7-07f0-4c9c-be8a-9dc00139cb83	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 for more than one week unless directed by a doctor Ask a doctor before use if you have abdominal pain, nausea or vomiting are taking mineral oil have noticed a sudden change in bowel habits that lasts over two weeks Stop use and ask a doctor if you have rectal bleeding or fail to have a bowel movement after 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.

Reported adverse events (FAERS/openFDA)#

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