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Mentholatum Kids Head Lice Removal Kit

FDA UDI

Class I (US FDA UDI)

by Mentholatum Company, The

Identity

Trade Name
Mentholatum Kids Head Lice Removal Kit FDA UDI
Generic Name
Lice treatment solution, synthetic FDA UDI
Device Name
One 3.38 FL OZ (100 mL) bottle with one lice comb. FDA UDI
Model / Reference
1123 FDA UDI
Description
One 3.38 FL OZ (100 mL) bottle with one lice comb. FDA UDI

Identifiers

Primary DI / UDI-DI
00310742011234 FDA UDI
FDA Product Code
LJL FDA UDI
GMDN Term
Lice treatment solution, synthetic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5960 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lice comb, manualLice treatment solution, synthetic

Mentholatum Kids Head Lice Removal Kit by Mentholatum Company, The — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lice treatment solution, synthetic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6c064ea9-bee9-4353-bf71-0a77ffd4e2d7 34 fields · synced May 30, 2026