Identity
- Trade Name
- B&C Ointment FDA UDI
- Generic Name
- Skin semi-occlusive dressing, non-antimicrobial FDA UDI
- Model / Reference
- 1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00316477502603 FDA UDI
- FDA Product Code
- NAC FDA UDI
- GMDN Term
- Skin semi-occlusive dressing, non-antimicrobial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4018 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
No
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: Skin semi-occlusive dressing, non-antimicrobial
B&C Ointment by Laser Pharmaceuticals — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin semi-occlusive dressing, non-antimicrobial.
- Simpurity — SAFE N SIMPLE LLC · Class I
- Simpurity — SAFE N SIMPLE LLC · Class I
- Simpurity — SAFE N SIMPLE LLC · Class I
- Simpurity — SAFE N SIMPLE LLC · Class I
- Simpurity — SAFE N SIMPLE LLC · Class I
- Simpurity — SAFE N SIMPLE LLC · Class I
- KeraStat Cream — Keranetics, LLC · U
- Simpurity — SAFE N SIMPLE LLC · Class I
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Laser Pharmaceuticals
Sources (1)
- FDA UDI 9a0688de-294f-404e-b636-b00957e5bb45 32 fields · synced May 31, 2026