NDC11 70108020401

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
70108-0204-01	70108-0204
70108-0204-1	70108-0204
70108-204-01	70108-204

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 ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT	SODIUM FLUORIDE	Ashtel Studios, Inc.	baae4f4a-54ef-472a-9c94-31703435750b	2025-07-01	Warnings	Exact identifier ndc (package): 70108-204-01 ndc (product): 70108-204 ndc11 (package): 70108020401

Reported adverse events (FAERS/openFDA)#

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