NDC11 67879030912

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
67879-0309-12	67879-0309
67879-309-12	67879-309

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
SUN THERAPE FACE AND BODY SPF-35	AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE	PHARMAGEL INTERNATIONAL INC	6a96623f-c37c-4e67-925e-f133461d726d	2024-08-13	Warnings	Exact identifier ndc (package): 67879-309-12 ndc (product): 67879-309 ndc11 (package): 67879030912

Reported adverse events (FAERS/openFDA)#

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