Home NDC 87204-164 FlyLeaf Fungal Nail Treatment
Product NDC 87204-164
11-digit product format 872040164
Labeler code 87204
Product ID 87204-164_49d8e823-b7a3-8c18-e063-6294a90a7745
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate 1%
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Huixue Biotechnology Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-02-02
Marketing end 2027-02-08
Substance TOLNAFTATE
Active strength 1 mg/15mL
NDC exclude flag No
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base FlyLeaf Fungal Nail Treatment Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE 1 mg/15mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 06KB629TKV Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 87204-164-01 FlyLeaf Fungal Nail Treatment 15 mL in 1 BOTTLE, PLASTIC LIQUID 15 1
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 8 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 87204-164-01 87204016401 15 mL in 1 BOTTLE, PLASTIC (87204-164-01) 15 ml 2026-02-02 2027-02-08 No No Historical