Home DailyMed fabc23eb-7750-1b5a-e053-6294a90aed03 Menthol Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer FSA Store Inc.
Effective date 2023-05-02
Label type HUMAN OTC DRUG LABEL
Version 1
Source legacy-cache
Hydrated at 2026-08-01 21:31:52 Label at a glance# Product Menthol
Active ingredient MENTHOL
Label structure 8 sections
Dosage and administration adults and children 2 years of age and older, apply to affected area not more than 3 to 4 times daily children under 2 years of age, consult a doctor wash and dry feet thoroughly sprinkle powder liberally on feet, between toes and on bottoms of feet
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 8 matching rows.
Menthol Maximum Strength Medicated Foot Powder Talc Free ZEA MAYS SUBSP. MAYS WHOLE TRICALCIUM PHOSPHATE SODIUM BICARBONATE BENZETHONIUM CHLORIDE EUCALYPTUS OIL PEPPERMINT OIL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 7 matching rows.
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Matched openFDA labels page 1 of 1 · 1 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.