NDC11 69423075223

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 NDCProduct root
69423-0752-2369423-0752
69423-752-2369423-752

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Crest 3D White AdvancedSODIUM MONOFLUOROPHOSPHATEThe Procter & Gamble Manufacturing Companyf3aa9a59-b4d4-05d9-e053-2995a90a0aea2026-01-08Exact identifier
ndc (package): 69423-752-23
ndc (product): 69423-752
ndc11 (package): 69423075223

Reported adverse events (FAERS/openFDA)#

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