LEADER DRY EYE RELIEF description, usages, side effects, indications, overdosage, supplying and lots more!

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LEADER DRY EYE RELIEF

Cardinal Health

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients                                                                          Purpose

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

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

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

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.

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

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of the reach of children.

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

Uses

Directions

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

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

DISTRIBUTED BY CARDINAL HEALTH

DUBLIN, OH 43017

CIN 1963776

www.myleader.com

1-800-200-6313

LEADER DRY EYE RELIEFEnter section text here

LEADER DRY EYE RELIEF

DEXTRAN, HYPROMELLOSE 2910 SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37205-603
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DEXTRAN 70 DEXTRAN 70 0.001 mL
HYPROMELLOSE 2910 (4000 MPA.S) 0.003 mL

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
potassium chloride
SODIUM BORATE
SODIUM CHLORIDE
BORIC ACID
water
SODIUM CHLORIDE
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:37205-603-05 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2012-01-04


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Be sure to consult your doctor before taking any medication!
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