Home NDC 77358-202 Bluevado Sunfix
Product NDC 77358-202
11-digit product format 773580202
Labeler code 77358
Product ID 77358-202_31f1e961-371a-f70a-e063-6394a90a481e
Type HUMAN OTC DRUG
Nonproprietary name Zinc Oxide, Titanium Dioxide
Dosage form LOTION
Route TOPICAL
Labeler Magic Blue, LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-05-31
Substance ZINC OXIDE; TITANIUM DIOXIDE
Active strength 15; 2.8 g/100mL; g/100mL
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 Bluevado Sunfix
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ZINC OXIDE 15 g/100mL TITANIUM DIOXIDE 2.8 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination SOI2LOH54Z Internal UNII lookup 15FIX9V2JP Internal UNII lookup
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 77358-202-03 Bluevado Sunfix 90 mL in 1 TUBE LOTION 90 3
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 77358-202-03 77358020203 90 mL in 1 TUBE (77358-202-03) 90 ml 2025-05-31 No No Current