Home NDC 84167-323 KONEUK SUNSCREEN SPF50
Product NDC 84167-323
11-digit product format 841670323
Labeler code 84167
Product ID 84167-323_48dd7f6e-2a4e-2c92-e063-6294a90a4255
Type HUMAN OTC DRUG
Nonproprietary name KONEUK SUNSCREEN SPF50
Dosage form CREAM
Route CUTANEOUS
Labeler Guangzhou Meixi Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-21
Substance OCTOCRYLENE; HOMOSALATE; TITANIUM DIOXIDE; AVOBENZONE; ENSULIZOLE
Active strength 1; 1; 1; 1; 1 g/1; g/1; g/1; g/1; g/1
NDC exclude flag No
Listing certified through 2027-12-31
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 KONEUK SUNSCREEN SPF50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OCTOCRYLENE 1 g/1 HOMOSALATE 1 g/1 TITANIUM DIOXIDE 1 g/1 AVOBENZONE 1 g/1 ENSULIZOLE 1 g/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
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 84167-323-03 KONEUK SUNSCREEN SPF50 5 in 1 BOX CREAM 5 1 84167-323-03 KONEUK SUNSCREEN SPF50 1 in 1 BOTTLE CREAM 1 1
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 84167-323-03 84167032303 5 BOTTLE in 1 BOX (84167-323-03) / 1 CREAM in 1 BOTTLE 5 bottle 2026-01-21 No No Current