Home NDC 85064-002 EELHOE Mole Reduce Essence
Product NDC 85064-002
11-digit product format 850640002
Labeler code 85064
Product ID 85064-002_448e4023-2dc4-06fc-e063-6294a90aa221
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form LIQUID
Route TOPICAL
Labeler Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-04
Substance CAMELLIA SINENSIS LEAF; MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
Active strength .002; .002 mg/10mg; mg/10mg
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 Mole Reduce Essence
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMELLIA SINENSIS LEAF .002 mg/10mg MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL .002 mg/10mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination W2ZU1RY8B0 Internal UNII lookup VIF565UC2G 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 85064-002-01 EELHOE Mole Reduce Essence 10 mg in 1 BOTTLE LIQUID 10 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85064-002 EELHOE MOLE REDUCE ESSENCE (SALICYLIC ACID) LIQUID [SHANTOU EELHOE DAILY CHEMICAL TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250306_2f80ffc4-c945-71c9-e063-6394a90add8c.zip
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 49 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 85064-002-01 85064000201 10 mg in 1 BOTTLE (85064-002-01) 10 mg 2025-03-04 No No Current