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 AND DOCUSATE SODIUM
Manufacturer: Medline Industries, LP
Product type: HUMAN OTC DRUG
SPL set ID: 6cd22881-db60-9045-e053-2991aa0ae08a
SPL ID: 536f49ab-7030-6114-e063-6394a90ad18e
Version: 9
Effective date: 2026-06-04
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 06:17:51

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 · 12 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 AND DOCUSATE SODIUM	openfda.generic_name
manufacturer name		Medline Industries, LP	openfda.manufacturer_name
ndc	package	53329-989-62	openfda.package_ndc
ndc	product	53329-989	openfda.product_ndc
ndc11	package	53329098962	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		536f49ab-7030-6114-e063-6394a90ad18e	id
spl set id		6cd22881-db60-9045-e053-2991aa0ae08a	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 this product if you are presently 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 a sudden change in bowel movements that persists over 2 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 could be signs of 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.