Identity
- Trade Name
- Neutrogena FDA UDI
- Generic Name
- Red/blue light phototherapy unit FDA UDI
- Device Name
- Light therapy acne mask FDA UDI
- Model / Reference
- 00070501260395 FDA UDI
- Description
- Light therapy acne mask FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00070501260395 FDA UDI
- FDA Product Code
- OLP FDA UDI
- GMDN Term
- Red/blue light phototherapy unit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Neutrogena by Kenvue Brands LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Kenvue Brands LLC
Sources (1)
- FDA UDI e11f3b76-4c74-46c7-9e19-e9a5e158f612 35 fields · synced May 30, 2026