Active Ingredients
Polysorbate 80 (1.0%)
Viva
FDA Label NDC 54891-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dakota Laboratories, Llc for the product Viva (NDC 54891-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Eye Lubricant
Keep Out Of Reach Of Children
• Keep this and all drugs out of the reach of children.
Indications & Usage
• Temporarily relieves burning and irritation due to dryness of the eye.
• Temporarily relieves discomfort due to minor irritations of the eye or to exposure to wind or sun.
• Protects against further irritation or relieves dryness of the eye.
• Lubricates to prevent further irritation or to relieve dryness of the eye.
Warnings
• To avoid contamination, do not touch tip of container to any surface.
• Replace cap after using
• If you experience pain, changes in vision, continued redness or irritation of the eye, or if the condition persists for more than 72 hours, discontinue use and consult a doctor.
• If solution changes color or becomes cloudy, do not use.
Dosage & Administration
Instill 1 or 2 drops in the affected eye(s) as needed.
Inactive Ingredient
purified water, sodium chloride, citric acid, edetate disodium with retinyl palmitate, mannitol, sodium citrate, and pyruvate as antioxidants.
* Please review the disclaimer below.
