FDA Label for Dry Eye Relief
View Indications, Usage & Precautions
Dry Eye Relief Product Label
The following document was submitted to the FDA by the labeler of this product Cardinal Health, 110 Dba Leader. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Purpose
| Active Ingredients | Purpose |
| Polyethylene Glycol 400 0.4% | Lubricant |
| Propylene Glycol 0.3% | Lubricant |
Uses
- for the temporary relief of burning and irritation due to dryness of the eye
- for use as a protectant against further irritation or to relieve dryness of the eye
Warnings
For external use only
Do Not Use
- if this product changes color or becomes cloudy
- if you are sensitive to any ingredient in this product
When Using This Product
- do not touch tip of container to any surface to avoid contamination
- replace cap after each use
Otc - Stop Use
Stop use and ask a doctor if you experience any of the following:
- you feel eye pain
- changes in vision
- continued redness or irritation of the eye
- condition worsens or persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- shake well before using
- put 1 or 2 drops in the affected eye(s) as needed
Other Information
- store at room temperature
Inactive Ingredients
boric acid, edetate disodium , potassium chloride, mangnesium chloride , sodium chloride, sodium borate , purified water. May contain hydrochloric acid and/or sodium hydroxide to adjust pH.
Package Label.Principal Display Panel
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