Home NDC 83789-572 Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine
Product NDC 83789-572
11-digit product format 837890572
Labeler code 83789
Product ID 83789-572_29954cb0-fccf-c278-e063-6394a90aa7c6
Type HUMAN OTC DRUG
Nonproprietary name TITANIUM DIOXIDE, ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler EK Clothing LLC dba Belasol
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-20
Substance TITANIUM DIOXIDE; ZINC OXIDE
Active strength 20; 170 mg/mL; mg/mL
Pharmacologic classes Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
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 Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TITANIUM DIOXIDE 20 mg/mL ZINC OXIDE 170 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 15FIX9V2JP Internal UNII lookup SOI2LOH54Z 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 83789-572-00 Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine 100 mL in 1 TUBE CREAM 100 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83789-572 BELASOL SUNCREAM NON TINTED MOISTURIZING SUNSCREEN SPF 50 JASMINE (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [EK CLOTHING LLC DBA BELASOL] 1 Current NDC, 1 package rows 20241228_e999d752-6c00-459e-b6c3-d264c330597d.zip
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 45 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 83789-572-00 83789057200 100 mL in 1 TUBE (83789-572-00) 100 ml 2024-11-20 No No Current