Active Ingredient
Menthol 1.0%
The following Structured Product Label (SPL) was submitted to the FDA by Davion, Inc for the product Maximum Strength Medicated Foot Powder (NDC 42669-283). 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, purpose, uses, warning, stop use and ask a doctor if, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Menthol 1.0%
External Analgesic
Temporary relief of pain and itch associated with:
In case of accidental ingestion, get medical help or contact a poison control center right away.
Remove seal beneath cap before first use. Do not use if seal is broken
For best results, dry skin throughly before applying
Zea Mays (Corn) Starch, Tricalcium Phosphate, Sodium Bicarbonate, Benzethonium Chloride, Eucalyptus Oil, Peppermint Oil
NDC 42669-283-01
CVS HEALTH Compared to the active ingredient in Maximum Strength Gold bond Medicated Foot Powder*
MAXIMUM STRENGTH Medicated Foot Powder WITH CORNSTARCG
NET WT 10 OZ (283 g)
* Please review the disclaimer below.