gudid
Primary ID: 00070501260364
Neutrogena (UDI 00070501260364)
Manufactured by Kenvue Brands LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Neutrogena - Primary ID 00070501260364
Device Regulatory Overview
The Neutrogena (Model/Catalog Number: 00070501260364) is a medical device manufactured by Kenvue Brands LLC. This product is indexed under FDA Product Code / Category Classification OLP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00070501260364
- Product Code / EMDN
- OLP
- Device Name
- Light therapy acne mask
- Database Sync Date
- 2026-08-09 09:08:47
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Neutrogena?
The registered manufacturer of record for Neutrogena is Kenvue Brands LLC.
What is the Primary UDI-DI identifier for Neutrogena?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00070501260364.
What classification code is assigned to this device?
This device is registered under product classification code OLP.
Similar Classification Devices (OLP)
Other Devices by Kenvue Brands LLC
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