Identity
- Trade Name
- Equate Liquid Bandage Sensitive Skin FDA UDI
- Generic Name
- Skin-cover sealant FDA UDI
- Device Name
- Liquid Bandage in a bottle with an applicator. FDA UDI
- Model / Reference
- 6398 FDA UDI
- Description
- Liquid Bandage in a bottle with an applicator. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00681131116398 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Skin-cover sealant
Equate Liquid Bandage Sensitive Skin by Walmart Stores — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin-cover sealant.
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
- Medline — MEDLINE INDUSTRIES, INC. · Class I
- CVS Liquid Bandage Spray — WOONSOCKET PRESCRIPTION CENTER, INCORPORATED · Class I
- McKesson — MCKESSON MEDICAL-SURGICAL INC. · Class I
- LiquidSkin, 1.0g — CHEMENCE MEDICAL INC. · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Meijer Blister Guard Spray — MEIJER, INC. · 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 |
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Manufacturer
- Manufacturer
- Walmart Stores
Sources (1)
- FDA UDI 6b86055d-4abc-4bef-9e39-7e014b0c7ca1 35 fields · synced Jun 8, 2026