NDC11 49967035601

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
49967-0356-01	49967-0356
49967-0356-1	49967-0356
49967-356-01	49967-356

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
NYX Professional Makeup Buttermelt Glaze SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30	HOMOSALATE,OCTISALATE AND OCTOCRYLENE	LOreal USA Products Inc	81093d80-dcaf-4555-98b2-48ce7eb84d0c	2024-12-23	Warnings	Exact identifier ndc (package): 49967-356-01 ndc (product): 49967-356 ndc11 (package): 49967035601

Reported adverse events (FAERS/openFDA)#

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