United States · FDA National Drug Code directory
APUREE Nailtific Extra-Max Strength Antigungal
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
- 84167-662_4a633da8-dcbb-349c-e063-6294a90a7702
- Product NDC
- 84167-662
- Form
- LIQUID
- Composition / generic term
- APUREE Nailtific Extra-Max Strength Antigungal
- Labeler
- Guangzhou Meixi Biotechnology Co., Ltd.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20260209
- Source listing expiry
- 20271231
Source-listed ingredients
- UNDECYLENIC ACID — .25 g/1
- TOLNAFTATE — .01 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 BOTTLE, PLASTIC in 1 BOX (84167-662-23) / 1 LIQUID in 1 BOTTLE, PLASTIC · 84167-662-23
Source and coverage
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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.
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