FDA.reportPublic FDA data

NDC11 14141033201

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
14141-0332-0114141-0332
14141-0332-114141-0332
14141-332-0114141-332

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
LBEL SPECIALISTE DARK SPOT BRIGHTENING MOISTURIZING SPF 30AVOBENZONE, OCTISALATE, OCTOCRYLENEBEL STAR SAfd90ffc6-a1e1-e02e-e053-6294a90a4e7c2024-10-28WarningsExact identifier
ndc (package): 14141-332-01
ndc (product): 14141-332
ndc11 (package): 14141033201

Reported adverse events (FAERS/openFDA)#

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