Active Ingredients (In Each Tablet)
Docusate sodium 50 mg
Sennosides 8.6 mg
The following Structured Product Label (SPL) was submitted to the FDA by Target Corporation for the product Stool Softener And Stimulant Laxative (NDC 11673-209). 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 ingredients (in each tablet), purpose, uses, warnings, do not use, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, 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
Stimulant laxative
DO NOT USE LAXATIVE PRODUCTS FOR LONGER THAN 1 WEEK UNLESS DIRECTED BY A DOCTOR IF YOU ARE PRESENTLY TAKING MINERAL OIL UNLESS DIRECTED BY A DOCTOR |
you have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
| adults and children 12 years and older | take 2-4 tablets daily |
| children 6 to under 12 years of age | take 1-2 tablets daily |
| children 2 to under 6 years of age | take up to 1 tablet daily |
| children under 2 | ask a doctor |
carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium benzoate, stearic acid, titanium dioxide
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