FDA.reportPublic FDA data

NDC11 82699020103

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
82699-0201-0382699-0201
82699-0201-382699-0201
82699-201-0382699-201

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
Dry Idea Advanced Dry Antiperspirant Roll-On, Powder FreshDRY IDEA ADVANCED DRY ANTIPERSPIRANT ROLL-ON, POWDER FRESHThriving Brands LLCf8335133-0299-b899-e053-6394a90a38372026-01-28WarningsExact identifier
ndc (package): 82699-201-03
ndc (product): 82699-201
ndc11 (package): 82699020103

Reported adverse events (FAERS/openFDA)#

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