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Eroxon

FDA UDI

Class II (US FDA UDI)

by Lil Drug Store Products, Inc.

Identity

Trade Name
Eroxon FDA UDI
Generic Name
Penile cooling/warming gel FDA UDI
Device Name
Eroxon is a clinically proven gel treatment for adult men with erectile dysfunction, or ED, which is the inability to get or keep an erection sufficient for satisfactory sexual activity. FDA UDI
Model / Reference
99990 FDA UDI
Description
Eroxon is a clinically proven gel treatment for adult men with erectile dysfunction, or ED, which is the inability to get or keep an erection sufficient for satisfactory sexual activity. FDA UDI

Identifiers

Catalog Number
99990 FDA UDI
Primary DI / UDI-DI
00792554999908 FDA UDI
510(k) Number
DEN220078 FDA UDI
FDA Product Code
QWW FDA UDI
GMDN Term
Penile cooling/warming gel FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5021 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Penile cooling/warming gel

Eroxon by Lil Drug Store Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Penile cooling/warming gel.

Cleared under the same submission

DEN220078 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lil Drug Store Products, Inc.

Sources (1)

  • FDA UDI 40e57095-bb06-4bbb-9129-0205c4193767 35 fields · synced Jun 6, 2026