Home NDC 85064-012 EELHOE Skin Advanced Mole Remove Serum
Product NDC 85064-012
11-digit product format 850640012
Labeler code 85064
Product ID 85064-012_448e4023-2dc7-06fc-e063-6294a90aa221
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 2025-09-17
Substance MELALEUCA ALTERNIFOLIA FLOWERING TOP; HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER
Active strength .006; .006 mg/30mg; mg/30mg
NDC exclude flag No
Listing certified through 2026-12-31
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 EELHOE Skin Advanced Mole Remove Serum
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MELALEUCA ALTERNIFOLIA FLOWERING TOP .006 mg/30mg HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER .006 mg/30mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5AZ4S6N66F Internal UNII lookup 8FP93ED6H2 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 85064-012-01 EELHOE Skin Advanced Mole Remove Serum 30 mg in 1 BOTTLE LIQUID 30 2
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 51 of 68 · 1,350 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85064-012-01 85064001201 30 mg in 1 BOTTLE (85064-012-01) 30 mg 2025-09-17 No No Current