RepHresh™ Vaginal Gel Personal Lubricant

FDA UDI

Class II (US FDA UDI)

by Church & Dwight Co., Inc.

Identity

Trade Name: RepHresh™ Vaginal Gel Personal Lubricant FDA UDI
Generic Name: Sexual lubricant FDA UDI
Model / Reference: 00022600019657 FDA UDI

Identifiers

Primary DI / UDI-DI: 00022600019657 FDA UDI
FDA Product Code: NUC FDA UDI
GMDN Term: Sexual lubricant FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.5300 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Sexual lubricant

RepHresh™ Vaginal Gel Personal Lubricant by Church & Dwight Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Church & Dwight Co., Inc.

Sources (1)

FDA UDI 2c71064c-aa27-4547-a57a-c4096edb87de 33 fields · synced Jun 9, 2026