United States · FDA National Drug Code directory

Menthol

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
82442-211_42f3fbdb-8110-35e8-e063-6394a90a5f53
Product NDC
82442-211
Form
POWDER
Composition / generic term
Maximum Strength Medicated Foot Powder Talc Free
Labeler
Target Corporation
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20250527
Source listing expiry
20261231

Source-listed ingredients

  • MENTHOL — 10 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 283 g in 1 BOTTLE, PLASTIC (82442-211-01) · 82442-211-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →