FDA.reportPublic FDA data

NDC11 65753010110

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
65753-0101-1065753-0101
65753-101-1065753-101

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 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SunX SPF 30/BugX WallmountSUNX SPF 30/BUGX WALLMOUNTCoreTex Products Inc08480b2a-a888-fb00-e063-6294a90a41ea2023-10-22WarningsExact identifier
ndc (package): 65753-101-10
ndc11 (package): 65753010110
CoreTex Sun X SPF 30 ThinAVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONECoreTex Products Inc980388b5-8314-3143-e053-2995a90a72882023-10-22WarningsExact identifier
ndc (product): 65753-101
SunX SPF 30/BugX WallmountSUNX SPF 30/BUGX WALLMOUNTCoreTex Products Inc0846946b-a05d-826c-e063-6294a90a0a0f2023-10-11WarningsExact identifier
ndc (package): 65753-101-10
ndc11 (package): 65753010110

Reported adverse events (FAERS/openFDA)#

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