FDA Label for Leader Lubricant Eye Drops
View Indications, Usage & Precautions
Leader Lubricant Eye Drops Product Label
The following document was submitted to the FDA by the labeler of this product Cardinal Health. 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 - Active Ingredient
Active ingredients-------------------------------------------------Purpose
Polyethylene Glycol 400 (0.4%)-----------------------------Lubricant
Propylene Glycol
(0.3%)---------------------------------------Lubricant
Otc - Purpose
Uses
For the temporary relief of burning and irritation due to eye
dryness.
Warnings
Warnings
For external use only.
Otc - Do Not Use
Do not use
- if solution changes color or becomes cloudy
- if you are sensitive or allergic to any ingredient in this
product
Otc - When Using
When using this product
- to avoid contamination, do not touch tip of container to any surface
- replace cap after each use
Otc - Stop Use
Stop use and ask a doctor if
- you experience eye pain
- changes in vision occur
- redness or irritation of the eye(s) gets worse or lasts 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 immediately.
Indications & Usage
Directions
- Put 1 or 2 drops in the affected eye/s as needed.
Inactive Ingredient
Inactive ingredients: Boric Acid, Calcium Chloride, Chlorhexidine
Gluconate, Hydrochloric Acid, Hydroxypropyl Guar,
Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Chloride, Zinc
Chloride
Dosage & Administration
DISTRIBUTED BY CARDINAL HEALTH
DUBLIN, OHIO 43017
CIN 4290730
www.myleader.com
1-800-200-6313
Package Label.Principal Display Panel
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