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

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LEADER EYE ITCH RELIEF DROPS

HANLIM PHARM. CO., LTD.
UNITED EXCHANGE CORP.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient                                             Purpose

Ketotifen (0.025%)..........................................Antihistamine

(Equivalent to ketotifen fumarate 0.035%)

Purpose

Use

Temporarily relieves itchy eyes due to pollen, ragweed, grass, animal hair and dander.

Warnings

Do not use

  • if solution changes color or becomes cloudy
  • if you are sensitive to any ingredient in this product
  • to treat contact lens related irritation


  • do not touch tip of container to any surface to avoid contamination
  • remove contact lenses before use
  • wait at least 10 minutes before reinserting contact lenses after use
  • replace cap after each use

Stop use and ask a doctor if you experience any of the following:

  • eye pain
  • changes in vision
  • redness of the eye
  • itching worsens or lasts for more than 72 hours

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Directions

  • Adults and children 3 years of age and older: Put 1 drop in the affected eye(s) twice daily, every 8-12 hours, no more than twice per day
  • Children under 3 years of age: Consult a doctor

Other information

  • Only for use in the eye
  • Store between 20o-25oC (68o to 77oF) (See USP controlled Room Temperature)
  • Do not use if cap seal ring is broken

Inactive ingredients

benzalkonium chloride 0.01%, glycerol, sodium hydroxide and/or hydrochloric acid, and water for injection

LEADER EYE ITCH RELIEF DROPSEnter section text here

LEADER EYE ITCH RELIEF DROPS

KETOTIFEN FUMARATE SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11716-1163
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Ketotifen Fumarate Ketotifen 0.345 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
GLYCERIN
SODIUM HYDROXIDE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 5 in 1 BOTTLE
2 NDC:11716-1163-7 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-04-21


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Be sure to consult your doctor before taking any medication!
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