Active Ingredient
Sodium chloride 0.9% (W/V)
Ohtrust Artifical Eyedrop Liquid
FDA Label NDC 70970-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nanoplus Limited (cayman) Taiwan Branch for the product Ohtrust Artifical Eyedrop (NDC 70970-008). 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 ingredient, purpose, warnings, uses, stop use and ask a doctor if:, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Lubricant (Artificial Tears)
Warnings
For external use only
- Do not use if solution changes color or becomes cloudy
- Do not touch the tip of the container to any surface to avoid contamination
Uses
- 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
Stop Use 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.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- To open, twist cap to remove
- Instill 1 to 2 drops in the affected eye(s) as needed
- Discard any unused portion
Other Information
- Store at 15-30°C (59-86°F)
- Do not use if tamper-evident seal is broken or missing
Inactive Ingredients
Purified water, sodium borate, potassium chloride, calcium chloride, magnesium chloride
* Please review the disclaimer below.
