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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Docusate Sodium (NDC 0363-8991). 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 other, active ingredient (in each liquid-filled capsule), purpose, uses, warnings, ask a doctor before use if you have, otc - do not use, stop use and ask a doctor if you, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Docusate Sodium 100 mg
Stool Softner laxative
Warnings
Do not use if you are presently taking mineral oil, unless told to do so by a doctor
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.1(800)222-1222
take with a glass of water
take by mouth. Doses may be taken as a single daily dose or in divided doses.
Adults and children 12 years and over | take 1 to 3 capsules daily. |
Children 2 to under 12 years of age | 1 capsule daily. |
Children under 2 years of age | Ask a doctor |
FD&C Red#40, FD&C Yellow#6, gelatin,glycerin, polyethylene glycol 400, propylene glycol, povidone, purified water, sorbitol solution, titanium dioxide.
1-888-333-9792
Compare to Dulcolax ® Stool Softener active ingredient *
GENTLE STOOL SOFTENER
DOCUSATE SODIUM 100 mg / STOOL SOFTENER LAXATIVE
25 LIQUID GELS
* Please review the disclaimer below.