GOODSENSE IRRITATION RELIEF EYE DROPS description, usages, side effects, indications, overdosage, supplying and lots more!

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GOODSENSE IRRITATION RELIEF EYE DROPS

HANLIM PHARM. CO., LTD.

DRUG FACTS




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients                                                                     Purpose

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

Zinc Sulfate.............................................................................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

Ask a doctor before use if you have narrow angle glaucoma

When using this product

  • pupils may become enlarged temporarily
  • overuse may cause more eye redness
  • remove contact lenses before using
  • do not use if this solution change color or becomes cloudy
  • 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 the eye 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 15o to 25oC (59o to 77oF)
  • Children under 6 years of age: Ask a doctor

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

GOODSENSE IRRITATION RELIEF EYE DROPSEnter section text here

GOODSENSE IRRITATION RELIEF EYE DROPS

TETRAHYDROZOLINE HYDROCHLORIDE ZINC SULFATE SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11716-0003
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:11716-0003-8 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-08-02


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Be sure to consult your doctor before taking any medication!
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