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Colgate Prorelief Sensitivity Relief Serum

FDA UDI

Class II (US FDA UDI)

by Colgate Oral Pharmaceuticals, Inc.

Identity

Trade Name
Colgate Prorelief Sensitivity Relief Serum FDA UDI
Generic Name
Dental cavity varnish FDA UDI
Device Name
Colgate ProRelief is designed for the management of sensitive teeth. The product is applied to any sensitive teeth with the Pro-Relief sonic applicator which the head is filled with serum and massaged on to each sensitive tooth. FDA UDI
Model / Reference
US05562A FDA UDI
Description
Colgate ProRelief is designed for the management of sensitive teeth. The product is applied to any sensitive teeth with the Pro-Relief sonic applicator which the head is filled with serum and massaged on to each sensitive tooth. FDA UDI

Identifiers

Primary DI / UDI-DI
00035000466426 FDA UDI
FDA Product Code
LBH FDA UDI
GMDN Term
Dental cavity varnish FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3260 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Colgate Prorelief Sensitivity Relief Serum by Colgate Oral Pharmaceuticals, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 877de8e7-a804-4d56-98a9-d622f535cd8b 35 fields · synced May 30, 2026