NDC11 62032091801

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
62032-0918-01	62032-0918
62032-0918-1	62032-0918
62032-918-01	62032-918

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
Obagi Nu-Derm System Normal-Dry Skin Transformation	HYDROQUINONE, TITANIUM DIOXIDE, AND ZINC OXIDE	Obagi Cosmeceuticals LLC	750ea9a6-eedc-49db-8cef-1498ed41ad79	2025-11-04	Warnings	Exact identifier ndc (package): 62032-918-01 ndc (product): 62032-918 ndc11 (package): 62032091801

Reported adverse events (FAERS/openFDA)#

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