Home DailyMed 7caef8db-a07a-6705-e053-2991aa0aa724 Top Care Menthol Foot Powder Talc Free 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 Topco Associates LLC
Effective date 2026-10-01
Label type HUMAN OTC DRUG LABEL
Version 8
Source daily-update
Hydrated at 2026-10-06 02:04:24 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
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DailyMed product names page 1 of 1 · 9 matching rows.
Menthol Maximum Strength Medicated Foot Powder Talc Free ZEA MAYS SUBSP. MAYS WHOLE TRICALCIUM PHOSPHATE EUCALYPTUS OIL SODIUM BICARBONATE BENZETHONIUM CHLORIDE PEPPERMINT OIL PEPPERMINT Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 7 matching rows.
Older Hydrated Versions# Version, Effective date, Source table Version Effective date Source Hydrated 7 2025-11-06 full-release 2026-06-01 01:42:39 6 2024-12-11 full-release 2026-06-01 00:42:28
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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.