Sennosides Tablets USP 8.6 mg

Manufacturer
InvaTech Pharma Solutions LLC | Elysium Pharmaceuticals Ltd
Effective date
2025-10-03
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:15:45

Label at a glance#

ProductSennosides
Active ingredientSENNA ALATA LEAF
Label structure7 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

FOR FURTHER MANUFACTURING, PROCESSING OR REPACKING

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN

INDICATIONS & USAGE SECTION

Laxative 

DOSAGE & ADMINISTRATION SECTION

FOR MANUFACTURING, PROCESSING OR REPACKING

WARNINGS SECTION

KEEP OUT OF THE REACH OF CHILDREN

INACTIVE INGREDIENT SECTION

Microcrystalline Cellulose, Dicalcium Phosphate, Croscarmellose Sodium, Stearic acid Powder, Colloidal Silicon Dioxide, Magnesium Stearate, Hypromellose, Polyethylene glycol, , Titanium dioxide, FD&C red

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57631-016-00Sennosides50000 in 1 BOXTABLET500004

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57631-01657631-016-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SennosidesSENNOSIDESInvaTech Pharma Solutions LLC3de39fbd-29be-fce7-e063-6394a90a67ae2025-10-03WarningsExact identifier
ndc (package): 57631-016-00
ndc (product): 57631-016
ndc11 (package): 57631001600
spl id: 403d9199-afba-4f1b-e063-6294a90aa7df
spl set id: 3de39fbd-29be-fce7-e063-6394a90a67ae

Reported adverse events (FAERS/openFDA)#

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