Home NDC 85064-034 Nail Renewal Liquid
Product NDC 85064-034
11-digit product format 850640034
Labeler code 85064
Product ID 85064-034_58d20060-43b0-03fb-e063-6294a90abb7c
Type HUMAN OTC DRUG
Nonproprietary name Glycerin
Dosage form LIQUID
Route TOPICAL
Labeler Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-03
Substance SOPHORA FLAVESCENS ROOT
Active strength .42 mg/30mg
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 Nail Renewal Liquid
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SOPHORA FLAVESCENS ROOT .42 mg/30mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination IYR6K8KQ5K 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 59 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85064-034-01 85064003401 30 mg in 1 BOTTLE, PLASTIC (85064-034-01) 30 mg 2026-08-03 No No Current