Home NDC 84148-021 Sunscreen SPF 50
Product NDC 84148-021
11-digit product format 841480021
Labeler code 84148
Product ID 84148-021_4dd1b4d9-8bf0-9713-e063-6294a90afe8e
Type HUMAN OTC DRUG
Nonproprietary name Sunscreen SPF 50
Dosage form CREAM
Route CUTANEOUS
Labeler Guangzhou Ariel Biotech Co., Ltd.
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-03-25
Substance ZINC OXIDE; SODIUM HYALURONATE; NIACINAMIDE; TITANIUM DIOXIDE
Active strength 15; .5; .5; 3 g/100g; g/100g; g/100g; g/100g
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 Sunscreen SPF 50
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 15 g/100g SODIUM HYALURONATE .5 g/100g NIACINAMIDE .5 g/100g TITANIUM DIOXIDE 3 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 84148-021-01 Sunscreen SPF 50 50 g in 1 BOTTLE CREAM 50 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 84148-021-01 84148002101 50 g in 1 BOTTLE (84148-021-01) 50 g 2026-03-25 No No Current