NDC11 70108021001

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
70108-0210-01	70108-0210
70108-0210-1	70108-0210
70108-210-01	70108-210

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
evo SENSITIVE WHITENING ANTI-CAVITY FLUORIDE	SODIUM FLUORIDE	Ashtel Studios, Inc.	1620c7fa-2af6-4462-af5d-9e122942788a	2025-07-15	Warnings	Exact identifier ndc (package): 70108-210-01 ndc (product): 70108-210 ndc11 (package): 70108021001

Reported adverse events (FAERS/openFDA)#

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