NDC11 49967001401

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
49967-0014-01	49967-0014
49967-0014-1	49967-0014
49967-014-01	49967-014

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
CeraVe Developed with Dermatologists Sunscreen Broad Spectrum SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	L'Oreal USA Products Inc	27d82e37-67ac-4cd3-83c0-fb8388d3a0dd	2023-12-31	Warnings	Exact identifier ndc (package): 49967-014-01 ndc (product): 49967-014 ndc11 (package): 49967001401

Reported adverse events (FAERS/openFDA)#

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