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

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LEADER RELIEF EYE

Cardinal Health

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients                                                                            Purpose

Tetrahydrozoline HCL 0.05% ...........................................................Redness Reliever

Zinc Sulfate 0.25% .........................................................................Astringent

Purpose

Uses

  • for the temporary relief of redness 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 eye pain
  • changes in vision occur
  • redness or irritation of 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) up to 4 times daily.
  • Store at room temperature.
  • Children under 6 years of age: Ask a doctor

Inactive Ingredients: Benzalkonium Chloride, Boric Acid, Edetate Disodium, Purified Water, Sodium Chloride, Sodium Citrate

Distributed By Cardinal Health

Dublin, OH 43017

CIN 1963735

www.myleader.com

1-800-200-6313

LEADER RELIEF EYEEnter section text here

LEADER RELIEF EYE

TETRAHYDROZOLINE HCL, ZINC SULFATE SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37205-138
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TETRAHYDROZOLINE HYDROCHLORIDE TETRAHYDROZOLINE 0.5 mg
ZINC SULFATE 2.5 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
BORIC ACID
EDETATE DISODIUM
water
SODIUM CHLORIDE
SODIUM CITRATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:37205-138-05 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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