Home NDC 87721-001 JELVOXA ANTIFUNGAL
Product NDC 87721-001
11-digit product format 877210001
Labeler code 87721
Product ID 87721-001_59a2f16e-ef73-f1cb-e063-6394a90abb28
Type HUMAN OTC DRUG
Nonproprietary name UNDECYLENIC ACID
Dosage form CREAM
Route TOPICAL
Labeler Wuhan Ruihengjie Technology Co., Ltd.
Application M005
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-22
Substance UNDECYLENIC ACID
Active strength 15 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 JELVOXA ANTIFUNGAL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength UNDECYLENIC ACID 15 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 1792394 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 8 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 87721-001-01 87721000101 120 mL in 1 BOTTLE (87721-001-01) 120 ml 2026-08-22 No No Current