NDC11 80684018001

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
80684-0180-0180684-0180
80684-0180-180684-0180
80684-180-0180684-180

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
B-Pure Hand SanitizerTropical Burst ScentedALCOHOLFourstar Group USA, Inc.67fe2f38-ed73-4fe7-9056-fa87f73004032025-12-02WarningsExact identifier
ndc (package): 80684-180-01
ndc (product): 80684-180
ndc11 (package): 80684018001

Reported adverse events (FAERS/openFDA)#

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