United States · FDA National Drug Code directory

APUREE Nailtific Maximum Strength Dual-Action Antifungal Pen Pro

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
84167-411_518abf2b-6ac9-ab9b-e063-6294a90ae693
Product NDC
84167-411
Form
LIQUID
Composition / generic term
APUREE Nailtific Maximum Strength Dual-Action Antifungal Pen Pro
Labeler
Guangzhou Meixi Biotechnology Co., Ltd.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20260511
Source listing expiry
20271231

Source-listed ingredients

  • UNDECYLENIC ACID — .25 g/1
  • TOLNAFTATE — 1 g/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 APPLICATOR in 1 BOX (84167-411-02) / 6 LIQUID in 1 APPLICATOR · 84167-411-02

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 →
APUREE Nailtific Maximum Strength Dual-Action Antifungal Pen Pro — United States | Molindra Medicines