Home NDC 87786-034 YAMANGU FUNGAL NAIL RENEWAL
Product NDC 87786-034
11-digit product format 877860034
Labeler code 87786
Product ID 87786-034_5843cc12-de67-ca47-e063-6294a90ae55b
Type HUMAN OTC DRUG
Nonproprietary name Undecylenic acid 25% FUNGAL NAIL RENEWAL
Dosage form LIQUID
Route TOPICAL
Labeler Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-05
Substance UNDECYLENIC ACID
Active strength 25 g/100mL
NDC exclude flag No
Listing certified through 2027-12-31
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 YAMANGU FUNGAL NAIL RENEWAL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength UNDECYLENIC ACID 25 g/100mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998329 Internal RxNorm 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 40 of 49 · 973 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87786-034-01 87786003401 2 BOTTLE in 1 BOX (87786-034-01) / 15 mL in 1 BOTTLE 2 bottle 2026-08-05 No No Current