NDC11 85735020350

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
85735-0203-50	85735-0203
85735-203-50	85735-203

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
Clear Path Tinted Facial Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	LULUS SPA BOUTIQUE	37657755-fa82-88a0-e063-6394a90ade47	2025-12-08		Exact identifier ndc (package): 85735-203-50 ndc (product): 85735-203 ndc11 (package): 85735020350

Reported adverse events (FAERS/openFDA)#

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