Home NDC 87204-190 Aiilo NAIL FUNGUS TREATMENT
Product NDC 87204-190
11-digit product format 872040190
Labeler code 87204
Product ID 87204-190_5689ac31-4d24-0fcc-e063-6394a90ac75b
Type HUMAN OTC DRUG
Nonproprietary name Undecylenic Acid 25%
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Huixue Biotechnology Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-04
Marketing end 2027-07-10
Substance UNDECYLENIC ACID
Active strength .25 mg/30mL
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 Aiilo NAIL FUNGUS TREATMENT Active Ingredients# Ingredient, Strength table Ingredient Strength UNDECYLENIC ACID .25 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K3D86KJ24N Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 87204-190-01 87204019001 30 mL in 1 BOTTLE, PLASTIC (87204-190-01) 30 ml 2026-07-04 2027-07-10 No No Historical