NDC 48878-3170 - 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
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 Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Clinpro Tooth Creme - Solventum US LLC | Sheffield Pharmaceuticals LLCSolventum US LLC | Sheffield Pharmaceuticals LLC2026-01-08HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48878-3170-1Clinpro Tooth Creme1 in 1 BOXPASTE, DENTIFRICE18
48878-3170-1Clinpro Tooth Creme113 g in 1 TUBEPASTE, DENTIFRICE1138
48878-3170-2Clinpro Tooth Creme1 in 1 BOXPASTE, DENTIFRICE18
48878-3170-2Clinpro Tooth Creme24 g in 1 TUBEPASTE, DENTIFRICE248
48878-3170-5Clinpro Tooth Creme113 g in 1 TUBEPASTE, DENTIFRICE1138
48878-3170-5Clinpro Tooth Creme1 in 1 BOXPASTE, DENTIFRICE18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48878-3170CLINPRO TOOTH CREME (SODIUM FLUORIDE) PASTE, DENTIFRICE [SOLVENTUM US LLC]76 package rows20240808_df0a06be-536b-4a8b-91bf-4d755adb345f.zip