NDC11 84821000250

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 NDC	Product root
84821-0002-50	84821-0002
84821-002-50	84821-002

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Byoma Ultralight Face Fluid SPF 30	AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	BYOMA LIMITED	2657bca4-bdc7-d959-e063-6394a90a2aa1	2024-11-07	Warnings	Exact identifier ndc (package): 84821-002-50 ndc (product): 84821-002 ndc11 (package): 84821000250

Reported adverse events (FAERS/openFDA)#

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