Identity
- Trade Name
- Walgreens FDA UDI
- Generic Name
- Multi-purpose soft contact lens solution FDA UDI
- Device Name
- Multi-Purpose Solution with Lens Case FDA UDI
- Model / Reference
- 066 FDA UDI
- Description
- Multi-Purpose Solution with Lens Case FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00311917200675 FDA UDI
- FDA Product Code
- LYL FDA UDI
- GMDN Term
- Multi-purpose soft contact lens solution 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 355 Milliliter FDA UDI
Category: Multi-purpose soft contact lens solution
Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Multi-purpose soft contact lens solution.
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- Bausch + Lomb — Bausch & Lomb Incorporated · Class II
- REVITALENS — Johnson & Johnson Surgical Vision, 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
- Walgreen Co.
Sources (1)
- FDA UDI 396b8223-1761-4c3a-9a50-0f7096fa1a27 35 fields · synced Jun 1, 2026