FDA UDI In Commercial Distribution 🇺🇸 United States

Eroxon

DI: 00792554999908 · Model: 99990 · Lil' Drug Store Products, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Eroxon
Primary DI
00792554999908
Version / Model
99990
Catalog Number
99990
Company Name
Lil' Drug Store Products, Inc.
Labeler DUNS
093103646
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2024-10-21
Public Version
1
Public Version Date
2024-10-29
Public Version Status
New
Public Device Record Key
40e57095-bb06-4bbb-9129-0205c4193767

Device 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.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QWW Non-Medicated Topical Formulation For Treatment Of Erectile Dysfunction.

GMDN Terms

Code Name
66929 Penile cooling/warming gel

Identifiers

Type ID
Unit of Use 00079255499990
Primary 00792554999908

Premarket Submissions

Submission Number Supplement Number
DEN220078 000