NDC11 78317002701

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
78317-0027-01	78317-0027
78317-0027-1	78317-0027
78317-027-01	78317-027

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
Dr.C.Tuna Sun Face Cream SPF50	AVOBENZONE, OCTINOXATE, HOMOSALATE, OCTOCRYLENE	Tan Alize Kozmetik ve Temizlik Urunleri Sanayi ve Ticaret Anonim Sirketi	f668c078-61e6-2c81-e053-2a95a90a3100	2023-11-05	Warnings	Exact identifier ndc (package): 78317-027-01 ndc (product): 78317-027 ndc11 (package): 78317002701

Reported adverse events (FAERS/openFDA)#

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