Identity
- Trade Name
- Johnson & Johnson First Aid FDA UDI
- Generic Name
- First aid kit, medicated FDA UDI
- Device Name
- J&J ALL-PURPOSE NEOSPORIN/BAND-AID L X 140 FIRST AID KIT FDA UDI
- Model / Reference
- 00381371172108 FDA UDI
- Description
- J&J ALL-PURPOSE NEOSPORIN/BAND-AID L X 140 FIRST AID KIT FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00381371172108 FDA UDI
- FDA Product Code
- LRR FDA UDI
- GMDN Term
- First aid kit, medicated FDA UDI
Classification
- Device Class
- N FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Johnson & Johnson First Aid by Kenvue Brands LLC — Class N — 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 N | Pending data |
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Manufacturer
- Manufacturer
- Kenvue Brands LLC
Sources (1)
- FDA UDI 4438fb55-8f36-4b7e-81f2-e3786e834a12 35 fields · synced May 30, 2026