Home NDC 80134-050-01 NDC 80134-050-01 - Brillie Ultimate Soothing Sun Shield This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 80134-050
Requested NDC 80134-050-01
Package NDCs from labels 80134-050-01, 80134-050-02
Manufacturer Inhanzglobal Co.,Ltd | BRILLIANT
Effective date 2020-08-21
Current FDA listing Not matched in FDA.report NDC product tables
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80134-050-01 Brillie Ultimate Soothing Sun Shield 50 mL in 1 TUBE CREAM 50 1 80134-050-02 Brillie Ultimate Soothing Sun Shield 1 in 1 BOX CREAM 1 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80134-050 BRILLIE ULTIMATE SOOTHING SUN SHIELD (ETHYLHEXYL METHOXYCINNAMATE, BENZOPHENONE-4, TITANIUM DIOXIDE) CREAM [INHANZGLOBAL CO.,LTD] 1 Legacy NDC, 2 package rows 20200824_ad620c86-60db-4428-e053-2a95a90aeb26.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 9 of 203 · 4,050 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.