Home NDC 85064-007 EELHOE Skin Tag Remover
Product NDC 85064-007
11-digit product format 850640007
Labeler code 85064
Product ID 85064-007_448e3e8d-50e2-fa4a-e063-6394a90abe1b
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 2025-04-12
Substance PLATYCLADUS ORIENTALIS LEAF
Active strength .006 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 Tag Remover
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PLATYCLADUS ORIENTALIS LEAF .006 mg/30mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 32E5V7G32B 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 85064-007-01 EELHOE Skin Tag Remover 30 mg in 1 BOTTLE LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85064-007 EELHOE SKIN TAG REMOVER (GLYCERIN) LIQUID [SHANTOU EELHOE DAILY CHEMICAL TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250413_32922508-74ae-8347-e063-6294a90a6154.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 53 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 85064-007-01 85064000701 30 mg in 1 BOTTLE (85064-007-01) 30 mg 2025-04-12 No No Current