Active Ingredient (In Each Softgel)
Docusate Sodium 50 mg
Sennosides 8.6 mg
The following Structured Product Label (SPL) was submitted to the FDA by Softgel Healthcare Private Limited for the product Docusate Sodium And Sennosides (NDC 35916-0454). 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 softgel), purpose, uses, warningsdo not use, ask a doctor before use if you have, stop use and ask a doctor if you have, 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
ask a health professional before use.
In case of accidental overdose, seek professional assistance or contact a Poison Control Center right away.
| Age | Starting Dosage | Maximum Dosage |
| adults and children 12 years of age and older | 2 softgels once a day | 4 softgels twice a day |
| children 6 to 12 years of age | 1 softgel once a day | 2 softgels twice a day |
| children under 6 years of age | ask a doctor | ask a doctor |
Propylene glycol, Povidone, Colloidal Silicon Dioxide, Yellow wax, Polyethylene glycol 400, Gelatin, Glycerin, Sorbitol Sorbitan Solution, FD&C Red No.40, Titanium dioxide and Purified water.
* Please review the disclaimer below.