Active Ingredient (In Each Softgel)
Docusate Sodium 250 mg
The following Structured Product Label (SPL) was submitted to the FDA by Amerisource Bergen for the product Stool Softener (NDC 46122-826). 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, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Docusate Sodium 250 mg
Stool Softener
Ask a doctor before use if you
Stop use and ask a doctor if
These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before
use.
Keep out of the reach of children. In case of accidental overdose,
get medical help or contact a Poison Control Center right away.
FD&C red #40, FD&C yellow #6 (sunset yellow), gelatin, glycerol, PEG, purified water, sorbitol special
1-800-540-3765
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