KamDoy Rx Skin Emulsion

FDA UDI

Class U (US FDA UDI)

by Alvix Laboratories, Llc

Identity

Trade Name: KamDoy Rx Skin Emulsion FDA UDI
Generic Name: Skin osmotic dressing, non-sterile FDA UDI
Device Name: KamDoy Rx Skin Emulsion is indicated as a prescription topical skin care emulsion to manage and relieve the burning and itching experienced with various types of dermatoses, including atopic and allergic contact dermatitis. KamDoy Rx Skin Emulsion helps maintain a moist wound and skin environment, which is beneficial to the healing process. FDA UDI
Model / Reference: FP1012-1 FDA UDI
Description: KamDoy Rx Skin Emulsion is indicated as a prescription topical skin care emulsion to manage and relieve the burning and itching experienced with various types of dermatoses, including atopic and allergic contact dermatitis. KamDoy Rx Skin Emulsion helps maintain a moist wound and skin environment, which is beneficial to the healing process. FDA UDI

Identifiers

Primary DI / UDI-DI: 00315455956612 FDA UDI
510(k) Number: K141637 FDA UDI
FDA Product Code: FRO FDA UDI
GMDN Term: Skin osmotic dressing, non-sterile FDA UDI

Classification

Device Class: U FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

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

MRI Safety

MR Unsafe FDA UDI

Category: Skin osmotic dressing, non-sterile

KamDoy Rx Skin Emulsion by Alvix Laboratories, Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin osmotic dressing, non-sterile.

Iliderm Rx Skin Emulsion — Levins Pharmaceuticals LLC · U

Cleared under the same submission

K141637 also covers:

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 U	Pending data

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Manufacturer

Manufacturer: Alvix Laboratories, Llc

Sources (1)

FDA UDI b2314fd0-18e4-4981-9c15-a70859a9559c 34 fields · synced May 30, 2026