Home NDC 85064-017 EELHOE Matte Sun Stick
Product NDC 85064-017
11-digit product format 850640017
Labeler code 85064
Product ID 85064-017_448e4dd3-cfdf-3b98-e063-6294a90a789e
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE
Dosage form CREAM
Route TOPICAL
Labeler Shantou Eelhoe Daily Chemical Technology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-05
Substance CAMELLIA JAPONICA FLOWER; ARTEMISIA VULGARIS ROOT
Active strength .054; .0036 mg/18mg; mg/18mg
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 Matte Sun Stick
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMELLIA JAPONICA FLOWER .054 mg/18mg ARTEMISIA VULGARIS ROOT .0036 mg/18mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination KUB8101TNF Internal UNII lookup 32MP823R8S 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 85064-017-01 EELHOE Matte Sun Stick 18 mg in 1 BOX CREAM 18 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 26 of 357 · 7,139 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85064-017-01 85064001701 18 mg in 1 BOX (85064-017-01) 18 mg 2025-11-05 No No Current