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Levicyn Antipruritic Spray Gel

FDA UDI

Class U (US FDA UDI)

by Sonoma Pharmaceuticals, Inc.

Identity

Trade Name
Levicyn Antipruritic Spray Gel FDA UDI
Generic Name
Wound hydrogel dressing, non-antimicrobial FDA UDI
Model / Reference
85020 FDA UDI

Identifiers

Catalog Number
85020 FDA UDI
Primary DI / UDI-DI
00860452000368 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, non-antimicrobial FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

Dimensions & Sizes

Size
Weight — 14 Gram FDA UDI

Category: Wound hydrogel dressing, non-antimicrobial

Levicyn Antipruritic Spray Gel by Sonoma Pharmaceuticals, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI debe69f6-d57c-4e83-9825-2b405c9e70d2 35 fields · synced May 30, 2026