Product Information
VISCOAT® Ophthalmic Viscoelastic Solution (OVD), 0.5 mL Prefilled Syringe — Alcon
Product Details
| Brand | VISCOAT® |
| Active Ingredients | Sodium chondroitin sulfate 40 mg/mL (4%) and sodium hyaluronate 30 mg/mL (3%) |
| Dosage Form | Sterile ophthalmic viscoelastic solution |
| Route of Administration | Intraocular use during ophthalmic surgery |
| Package Size | 0.5 mL single-use prefilled syringe |
| Manufacturer | Alcon |
| NDC | 08065-1839-05 |
Description
VISCOAT® Ophthalmic Viscoelastic Solution is a sterile ophthalmic viscoelastic device designed to assist qualified ophthalmic surgeons during anterior segment procedures. Its combination of sodium chondroitin sulfate and sodium hyaluronate helps maintain anterior chamber depth and protect ocular tissues during surgery.
Indications and Usage
VISCOAT® is indicated for use as an ophthalmic surgical aid in anterior segment procedures, including cataract extraction and intraocular lens (IOL) implantation. It helps maintain anterior chamber depth, improve visualization during surgery, and protect the corneal endothelium and other ocular tissues.
Dosage and Administration
For use by qualified ophthalmic surgeons during anterior segment procedures. The amount used depends on the surgical technique and the surgeon's clinical judgment. Administer intraocularly according to the manufacturer's instructions for use.
Warnings and Precautions
- For intraocular surgical use by qualified ophthalmic professionals only.
- Follow the manufacturer's instructions for assembly and use of the supplied cannula.
- Failure to follow assembly instructions or use of an alternate cannula may result in cannula detachment and potential patient injury.
- Refer to the manufacturer's complete instructions for use for all warnings and precautions.
Contraindications
Refer to the manufacturer's instructions for use for applicable contraindications and precautions.
Adverse Reactions
Potential risks are associated with intraocular surgery and the use of ophthalmic viscoelastic devices. Refer to the product's complete instructions for use for detailed safety information.
Storage and Handling
Store according to the manufacturer's labeled storage conditions. This product may require refrigeration; verify the storage requirements on the product packaging before handling.
How Supplied
VISCOAT® Ophthalmic Viscoelastic Device is supplied as a sterile, single-use, prefilled syringe containing 0.5 mL of solution with 4% sodium chondroitin sulfate and 3% sodium hyaluronate.
NDC: 08065-1839-05
Professional Use Only. Clinical information is summarized from Alcon product information and is provided for reference. Refer to the manufacturer's complete instructions for use for full prescribing, safety, handling, and storage details.
If you have any questions related to DSCSA compliance, transaction history, regulatory data, or quality assurance, please contact our team at compliance@dryeyerescue.com for more information.
CLINIC ESSENTIALS
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NDC 24208-730-06
NDC 24208-585-64
NDC 24208-295-25
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