NDC11 50390010830

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
50390-0108-30	50390-0108
50390-108-30	50390-108

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ARTISTRY IDEAL RADIANCE UV Protect SPF 50 PLUS Broad Spectrum Sunscreen	OCTINOXATE, OCTISALATE, ZINC OXIDE, TITANIUM DIOXIDE	Amway Corp	a1a700b5-d039-4bd2-8420-5c2053095706	2024-01-02	Warnings	Exact identifier ndc (package): 50390-108-30 ndc (product): 50390-108 ndc11 (package): 50390010830

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.