Otc - Active Ingredient
Active ingredient (in each softgel)
Docusate sodium USP 50 mg
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Pharmacy for the product Docusate Sodium 50mg Softgel (red) (NDC 51316-651). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - pregnancy or breast feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Active ingredient (in each softgel)
Docusate sodium USP 50 mg
Purpose
Stool softener
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, 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).
Directions
adults and children 12 years and over | take 1-6 softgels daily |
children 2 to under 12 years of age | take 1-3 softgels daily |
| children under 2 years | ask a doctor |
Other information
Inactive ingredients D&C red 33, FD&C blue 1, FD&C red no. 40, FD&C yellow no. 6, gelatin, glycerin, noncrystallizing sorbitol solution, polyethylene glycol, propylene glycol, purified water, shellac, titanium dioxide
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