FDA.reportPublic FDA data

NDC11 73251001001

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 NDCProduct root
73251-0010-0173251-0010
73251-0010-173251-0010
73251-010-0173251-010

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Purito Sunday Adventure Sunscreen SPF 50, 50 mLAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEHinaturebf16f535-97fc-4fd8-9310-8b6bbc82baae2026-03-31WarningsExact identifier
ndc (package): 73251-010-01
ndc (product): 73251-010
ndc11 (package): 73251001001

Reported adverse events (FAERS/openFDA)#

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