Otc - Active Ingredient
Sodium chloride 0.9%
The following Structured Product Label (SPL) was submitted to the FDA by Water Beauty Innovation Co. Ltd. for the product Artificial Eyedrop (NDC 87406-003). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Sodium chloride 0.9%
Lubricant
• Relieves dryness and irritation of the eye
• Provides temporary relief from discomfort due to minor eye irritations or exposure to wind or sun
• Helps protect against further eye irritation
• For external use only
• Do not touch the tip of the container to any surface to avoid contamination
• If swallowed, get medical help or contact a Poison Control Center right away
if solution changes color or becomes cloudy
if you are allergic to any of the ingredients
and ask a doctor if
– you experience eye pain
– changes in vision, continued redness, or irritation of the eye
– condition worsens or persists for more than 72 hours
• Keep out of reach of children
• To open, twist cap to remove
• Instill 1 to 2 drops in the affected eye(s) as needed
• Discard if solution changes color or becomes cloudy
• Store at 15–30°C (59–86°F)
• Do not use if tamper-evident seal is broken or missing
Purified water, sodium borate, potassium chloride, calcium chloride, magnesium chloride
* Please review the disclaimer below.