NDC11 44717008301

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
44717-0083-01	44717-0083
44717-0083-1	44717-0083
44717-083-01	44717-083

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
Illuminizing Blendrops Broad Spectrum SPF 40	HOMOSALATE, OCTISALATE, ZINC OXIDE	Wasatch Product Development, LLC	124e6702-97a4-95bf-e063-6394a90afc0d	2025-10-16	Warnings	Exact identifier ndc (package): 44717-083-01 ndc (product): 44717-083 ndc11 (package): 44717008301

Reported adverse events (FAERS/openFDA)#

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