Home NDC 84167-828 MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50
Product NDC 84167-828
11-digit product format 841670828
Labeler code 84167
Product ID 84167-828_5a0b4bd2-f6ae-35dc-e063-6294a90a8a66
Type HUMAN OTC DRUG
Nonproprietary name SUNSCREEN SPF50
Dosage form CREAM
Route EXTRACORPOREAL
Labeler Guangzhou Meixi Biotechnology Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-28
Substance BEMOTRIZINOL; ENSULIZOLE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; TITANIUM DIOXIDE
Active strength .015; .02; .017; .01; .08; .008 g/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 MZANK SUNSCREEN DAILY ULTIMATE PROTECTION SPF50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BEMOTRIZINOL .015 g/1 ENSULIZOLE .02 g/1 HOMOSALATE .017 g/1 OCTISALATE .01 g/1 OCTOCRYLENE .08 g/1 TITANIUM DIOXIDE .008 g/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 6 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 162 of 353 · 7,049 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84167-828-01 84167082801 36 BAG in 1 BOX (84167-828-01) / 1 CREAM in 1 BAG 36 bag 2026-08-28 No No Current