Home NDC 85248-020 Lepnuns MILIA REMOVER
Product NDC 85248-020
11-digit product format 852480020
Labeler code 85248
Product ID 85248-020_5707b633-5814-2c14-e063-6394a90afb77
Type HUMAN OTC DRUG
Nonproprietary name Didecyl dimethyl Ammonium Chloride 0.025% MILIA REMOVER
Dosage form LIQUID
Route TOPICAL
Labeler Jiangxi Yudexi Pharmaceutical Co., LTD
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-29
Substance DIDECYLDIMONIUM CHLORIDE
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 Lepnuns MILIA REMOVER
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIDECYLDIMONIUM CHLORIDE .25 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination JXN40O9Y9B Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85248-020-01 Lepnuns MILIA REMOVER 30 mL in 1 BOTTLE LIQUID 30 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 14 of 55 · 1,088 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85248-020-01 85248002001 30 mL in 1 BOTTLE (85248-020-01) 30 ml 2026-01-29 No No Current