NDC11 78863123002

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
78863-1230-02	78863-1230
78863-1230-2	78863-1230

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
NOON Cartessa Accelerate Program	ALLANTOIN, TITANIUM DIOXIDE, OCTOCRYLENE, AND AVOBENZONE	Noon Aesthetics M.R. Ltd	400ead81-ab07-400f-b261-db330e0fd004	2025-01-14	Warnings	Exact identifier ndc (package): 78863-1230-2 ndc11 (package): 78863123002
NOON Post Procedure Program	ALLANTOIN, TITANIUM DIOXIDE, OCTOCRYLENE, AND AVOBENZONE	Noon Aesthetics M.R. Ltd	9d1d11b4-40ff-4ea8-a3af-655f457c05f1	2025-01-14	Warnings	Exact identifier ndc (package): 78863-1230-2 ndc11 (package): 78863123002

Reported adverse events (FAERS/openFDA)#

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