FDA.reportPublic FDA data

NDC11 10893053004

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
10893-0530-0410893-0530
10893-0530-410893-0530
10893-530-0410893-530

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
Naturasil Mite B Gone TREATMENT KitSULFUR, THUJA OCCIDENTALISNature's Innovation, Inc.21ddffb1-6d71-4460-a79c-90e2d65a2bd32024-02-07WarningsExact identifier
ndc (package): 10893-530-04
ndc11 (package): 10893053004
Naturasil Mite B GoneSULFURNature's Innovation, Inc.d15c2ac6-f323-41af-adfe-f4c88427ffdb2024-01-18WarningsExact identifier
ndc (package): 10893-530-04
ndc (product): 10893-530
ndc11 (package): 10893053004

Reported adverse events (FAERS/openFDA)#

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