FDA.reportPublic FDA data

NDC11 60232004401

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
60232-0044-0160232-0044
60232-0044-160232-0044
60232-044-0160232-044

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
Physical Sunscreen SPF50 80 min WR 159-100TITANIUM DIOXIDE, TITANIUM DIOXIDE SUNSCREENSwiss-American CDMO, LLC0cca7b65-e24a-429c-b157-5f4e343424ab2023-11-09WarningsExact identifier
ndc (package): 60232-0044-1
ndc (product): 60232-0044
ndc11 (package): 60232004401

Reported adverse events (FAERS/openFDA)#

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