NDC11 51346053201

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
51346-0532-01	51346-0532
51346-0532-1	51346-0532
51346-532-01	51346-532

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
CALIFORNIA ALOE FRESH POW DERY SUN	HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE	NATURE REPUBLIC CO., LTD.	aa10dbbf-97b3-4258-bbd3-0d8cc9935e12	2026-01-13	Warnings	Exact identifier ndc (package): 51346-532-01 ndc (product): 51346-532 ndc11 (package): 51346053201

Reported adverse events (FAERS/openFDA)#

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