NDC11 30807106002

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
30807-1060-02	30807-1060
30807-1060-2	30807-1060

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
ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN	SPF50	Wild Child Laboratories PTY Ltd	2767ba3e-7434-d474-e063-6294a90aa4ff	2026-01-06	Warnings	Exact identifier ndc (package): 30807-1060-2 ndc (product): 30807-1060 ndc11 (package): 30807106002

Reported adverse events (FAERS/openFDA)#

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