FDA.reportPublic FDA data

NDC11 00135058205

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
00135-0582-0500135-0582
00135-0582-500135-0582
00135-582-0500135-582
0135-0582-050135-0582

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CHILDRENS FLONASE ALLERGY RELIEFFLUTICASONE PROPIONATEHaleon US Holdings LLCfab7a1f4-75e0-416f-9644-07aff08e6ab02024-03-05WarningsExact identifier
ndc (product): 0135-0582
CHILDRENS FLONASE ALLERGY RELIEFFLUTICASONE PROPIONATEHaleon US Holdings LLC3adff80f-fca7-4cc5-b106-0f68f71c85b02024-02-08WarningsExact identifier
ndc (package): 0135-0582-05
ndc (product): 0135-0582
ndc11 (package): 00135058205

Reported adverse events (FAERS/openFDA)#

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