Yeast Gard Advanced Suppository
FDA Label NDC 68093-7106

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Wisconsin Pharmacal Company for the product Yeast Gard Advanced (NDC 68093-7106). 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, purpose, indications & usage, warnings, otc - stop use, otc - pregnancy or breast feeding, otc - keep out of reach of children, otc - ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Directions

Remove one suppository from the foil wrap and place in the applicator.  Insert suppository into the vagina with the applicator.  Remove applicator and cleanse thoroughly with soap and water.  Use one suppository daily for seven days.

Inactive Ingredients

Bacillus coagulans, Polyethylene Glycols

Questions Or Comments?

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