Home NDC 87204-161 QQE Fungal Nail Treatment
Product NDC 87204-161
11-digit product format 872040161
Labeler code 87204
Product ID 87204-161_499c0bab-e7c7-9f20-e063-6294a90aae8b
Type HUMAN OTC DRUG
Nonproprietary name Tolnaftate 1%
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Huixue Biotechnology Co., Ltd.
Application M029
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-30
Marketing end 2027-02-05
Substance TOLNAFTATE
Active strength .15 mg/15g
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 QQE Fungal Nail Treatment Active Ingredients# Ingredient, Strength table Ingredient Strength TOLNAFTATE .15 mg/15g
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 87204-161-01 QQE Fungal Nail Treatment 15 g 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 1 of 1 · 2 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 87204-161-01 87204016101 15 g in 1 BOTTLE, PLASTIC (87204-161-01) 15 g 2026-01-30 2027-02-05 No No Historical