FDA Label for Leader Dry Eye Relief

Otc - Active Ingredient

Active Ingredients                                                                          Purpose

Dextran 70 (0.1%).........................................................................(Lubricant)

Hypromellose 2910 (0.3%).............................................................(Lubricant)

Otc - Purpose

Uses

• for the temporary relief of burning and irritation of the eye and for use as a protectant against further irritation.
• for the temporary relief of discomfort due to minor irritations of the eye or to exposure to wind or sun.
  

Warnings

Warnings

For external use only. Do not use: If this solution changes color or becomes cloudy or if you are sensitive to any ingredient in this product.

Otc - When Using

When using this product

• remove contact lenses before using
• 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 feel pain
  
• changes in vision occur
• redness or irritation of the eye gets worse or lasts more than 72 hours
  

Otc - Pregnancy Or Breast Feeding

If pregnant or breast-feeding,

ask a health professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

Directions

• Instill 1 or 2 drops in the affected eye(s) as needed.
• Store at room temperature
  

Inactive Ingredient

Inactive Ingredients: Benzalkonium Chloride, Potassium Chloride, Disodium Chloride, Sodium Borate, Sodium Chloride, Boric Acid, Sterile Water, Purified Water, Sodium Chloride, and Sodium Citrate

Dosage & Administration

DISTRIBUTED BY CARDINAL HEALTH

DUBLIN, OH 43017

CIN 1963776

www.myleader.com

1-800-200-6313

Package Label.Principal Display Panel

image of carton label - LeaderDryEyeReliefEyeDrops