Home NDC 48878-3170-2 NDC 48878-3170-2 - Clinpro Tooth Creme This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 48878-3170
Requested NDC 48878-3170-2
Package NDCs from labels 48878-3170-1, 48878-3170-2, 48878-3170-5
Manufacturer Solventum US LLC | Sheffield Pharmaceuticals LLC
Effective date 2026-01-08
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48878-3170-1 Clinpro Tooth Creme 1 in 1 BOX PASTE, DENTIFRICE 1 8 48878-3170-1 Clinpro Tooth Creme 113 g in 1 TUBE PASTE, DENTIFRICE 113 8 48878-3170-2 Clinpro Tooth Creme 1 in 1 BOX PASTE, DENTIFRICE 1 8 48878-3170-2 Clinpro Tooth Creme 24 g in 1 TUBE PASTE, DENTIFRICE 24 8 48878-3170-5 Clinpro Tooth Creme 113 g in 1 TUBE PASTE, DENTIFRICE 113 8 48878-3170-5 Clinpro Tooth Creme 1 in 1 BOX PASTE, DENTIFRICE 1 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48878-3170 CLINPRO TOOTH CREME (SODIUM FLUORIDE) PASTE, DENTIFRICE [SOLVENTUM US LLC] 7 6 package rows 20240808_df0a06be-536b-4a8b-91bf-4d755adb345f.zip
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 39 of 203 · 4,056 matching rows.
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Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.