Home NDC 85064-005 EELHOE Wart Remover
Product NDC 85064-005
11-digit product format 850640005
Labeler code 85064
Product ID 85064-005_448e437c-7b74-fd6c-e063-6294a90a08d2
Type HUMAN OTC DRUG
Nonproprietary name GLYCERIN
Dosage form OINTMENT
Route TOPICAL
Labeler Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-03-25
Substance SAFFLOWER; ARNICA MONTANA FLOWER
Active strength .004; .004 mg/20mg; mg/20mg
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 Wart Remover
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SAFFLOWER .004 mg/20mg ARNICA MONTANA FLOWER .004 mg/20mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 4VBL71TY4Y Internal UNII lookup OZ0E5Y15PZ Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85064-005-01 EELHOE Wart Remover 20 mg in 1 BOX OINTMENT 20 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85064-005 EELHOE WART REMOVER (GLYCERIN) OINTMENT [SHANTOU EELHOE DAILY CHEMICAL TECHNOLOGY CO., LTD.] 1 Current NDC, 1 package rows 20250327_3127d616-1933-e783-e063-6294a90a52f7.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 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 85064-005-01 85064000501 20 mg in 1 BOX (85064-005-01) 20 mg 2025-03-25 No No Current