Home NDC 85064-010 EELHOE Bodyacne Removal Cleanser
Product NDC 85064-010
11-digit product format 850640010
Labeler code 85064
Product ID 85064-010_448e4023-2dc6-06fc-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 2025-08-07
Substance ALOE BARBADENSIS LEAF
Active strength .024 mg/120mg
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 Bodyacne Removal Cleanser
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALOE BARBADENSIS LEAF .024 mg/120mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination ZY81Z83H0X 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 85064-010-01 EELHOE Bodyacne Removal Cleanser 120 mg in 1 BOX LIQUID 120 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 44 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 85064-010-01 85064001001 120 mg in 1 BOX (85064-010-01) 120 mg 2025-08-07 No No Current