Identity
- Trade Name
- REFRESH RELIEVA FOR CONTACTS FDA UDI
- Generic Name
- Eye lubricant FDA UDI
- Device Name
- REFRESH RELIEVA FOR CONTACTS Lubricant Eye Drops FDA UDI
- Model / Reference
- 96632 FDA UDI
- Description
- REFRESH RELIEVA FOR CONTACTS Lubricant Eye Drops FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00300236632083 FDA UDI
- 510(k) Number
- K190674 FDA UDI
- FDA Product Code
- LPN FDA UDI
- GMDN Term
- Eye lubricant FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5928 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye lubricant
Refresh Relieva For Contacts by Allergan — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye lubricant.
- Clear Eyes® — MEDTECH PRODUCTS, INC. · Class II
- SYSTANE — Alcon Laboratories, Inc. · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Allergan
Sources (1)
- FDA UDI 6203d410-1f05-4d30-a0bb-a24be6d7613e 36 fields · synced May 30, 2026