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: SENNA AND DOCUSATE SODIUM TABLETS, 8.6 MG AND 50 MG
Manufacturer: HealthLife of USA LLC
Product type: HUMAN OTC DRUG
SPL set ID: 02a5299c-4b0d-47ac-9838-afd0b0fdd4a6
SPL ID: 083396b6-6a49-ffc7-e063-6294a90ad8e2
Version: 9
Effective date: 2023-10-21
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:00

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 · 22 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		SENNA AND DOCUSATE SODIUM TABLETS, 8.6 MG AND 50 MG	openfda.generic_name
manufacturer name		HealthLife of USA LLC	openfda.manufacturer_name
ndc	package	69517-131-50	openfda.package_ndc
ndc	package	69517-131-05	openfda.package_ndc
ndc	package	69517-131-10	openfda.package_ndc
ndc	package	69517-131-02	openfda.package_ndc
ndc	package	69517-131-24	openfda.package_ndc
ndc	package	69517-131-25	openfda.package_ndc
ndc	product	69517-131	openfda.product_ndc
ndc11	package	69517013102	derived:openfda.package_ndc
ndc11	package	69517013125	derived:openfda.package_ndc
ndc11	package	69517013150	derived:openfda.package_ndc
ndc11	package	69517013124	derived:openfda.package_ndc
ndc11	package	69517013105	derived:openfda.package_ndc
ndc11	package	69517013110	derived:openfda.package_ndc
rxcui		998740	openfda.rxcui
spl id		083396b6-6a49-ffc7-e063-6294a90ad8e2	id
spl set id		02a5299c-4b0d-47ac-9838-afd0b0fdd4a6	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 lasts 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 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.