Identity
- Trade Name
- CVS Liquid Bandage Spray FDA UDI
- Generic Name
- Skin-cover sealant FDA UDI
- Device Name
- Liquid Bandage in aerosol can FDA UDI
- Model / Reference
- 276670 FDA UDI
- Description
- Liquid Bandage in aerosol can FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00050428617656 FDA UDI
- FDA Product Code
- NEC FDA UDI
- GMDN Term
- Skin-cover sealant FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5090 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Skin-cover sealant
CVS Liquid Bandage Spray by Woonsocket Prescription Center, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Skin-cover sealant.
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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 |
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Manufacturer
- Manufacturer
- Woonsocket Prescription Center, Incorporated
Sources (1)
- FDA UDI 2e53328f-7255-484a-a1c5-2b7292b63cd1 33 fields · synced Jun 8, 2026