Active Ingredient (In Each Tablet)
Docusate Sodium 50 mg
Sennosides 8.6 mg
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health 107, Llc for the product Sennosides And Docusate Sodium (NDC 55154-2578). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, warnings, ask a doctor before use if you, stop use and ask a doctor if, if pregnant or breast-feeding,, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Docusate Sodium 50 mg
Sennosides 8.6 mg
Stool softener
Laxative
Do not use for more than one week unless directed by a doctor.
you have rectal bleeding or fail to have a bowel movement after use of a laxative.
These may indicate a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
cellulose, croscarmellose sodium, dicalcium phosphate, FD&C yellow #6 lake, hypromellose, magnesium stearate, PEG, silica, talc, titanium dioxide.
Distributed by:
American Health Packaging, Columbus, Ohio 43217
762201
Distributed By:
Cardinal Health
Dublin, OH 43017
L58458880723
0462201/0621A
* Please review the disclaimer below.