NDC11 67879030851

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
67879-0308-51	67879-0308
67879-308-51	67879-308

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
DERMA BRITE SPF 35	OCTINOXATE, OCTISALATE, OXYBENZONE	PHARMAGEL INTERNATIONAL INC	fe10912e-00e3-406c-a80c-d9c991dc9f8b	2024-08-13	Warnings	Exact identifier ndc (package): 67879-308-51 ndc (product): 67879-308 ndc11 (package): 67879030851

Reported adverse events (FAERS/openFDA)#

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