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: DOCUSATE SODIUM, SENNOSIDES
Manufacturer: Safeway, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: acb40b29-5fd5-4864-b6bf-4102e47a1683
SPL ID: 7645f18f-a849-4fc6-9661-0591c511bae6
Version: 5
Effective date: 2026-01-05
Source export date: 2026-09-28
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:12:36

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		505G(a)(3)	openfda.application_number
brand name		Senna S	openfda.brand_name
generic name		DOCUSATE SODIUM, SENNOSIDES	openfda.generic_name
manufacturer name		Safeway, Inc.	openfda.manufacturer_name
ndc	package	21130-883-30	openfda.package_ndc
ndc	product	21130-883	openfda.product_ndc
ndc11	package	21130088330	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		7645f18f-a849-4fc6-9661-0591c511bae6	id
spl set id		acb40b29-5fd5-4864-b6bf-4102e47a1683	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 if you are now 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 noticed a sudden change in bowel habits that continues over a period of 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 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.