Gericare Artificial Tears Lubricant Eye description, usages, side effects, indications, overdosage, supplying and lots more!

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Gericare Artificial Tears Lubricant Eye

Gericare Pharmaceuticals

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients                                                               Purpose

Glycerin 0.2%...................................................................Lubricant

Hypromellose 0.2%...........................................................Lubricant

Polyethylene glycol 400 1%...............................................Lubricant

Purpose

Uses

  • for the temporary relief of burning and irritation due to dryness of the eye
  • for protection against further irritation

Warnings For external use only

When using this product

  • remove contact lenses before using
  • do not use this solution if it changes color or becomes cloudy
  • avoid contamination: do not touch tip of container to any surface
  • replace cap after each use
  • some users may experience a brief tingling sensation

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts or gets worse

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

  • adults and children 12 years and older: put 1 to 2 drops in the affected eye(s) up to 3 times daily
  • children under 12 years of age: ask a doctor

Other information

  • store at room temperature 15°-25°C (59°-77°F)

Inactive ingredients: benzalkonium chloride, boric acid, dextrose, glycine, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium citrate, and sodium lactate

Distributed By:

Gericare Pharmaceuticals Corp.

Brooklyn, NY 11204

Made in Korea

Gericare Artificial Tears Lubricant Eye

Gericare Artificial Tears Lubricant Eye

Glycerin SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57896-184
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
GLYCERIN 0.002 mg
HYPROMELLOSES 0.002 mg
polyethylene glycol 400 Polyethylene Glycol 400 0.01 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
BORIC ACID
DEXTROSE
glycine
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM BORATE
SODIUM CHLORIDE
SODIUM CITRATE
sodium lactate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:57896-184-05 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2013-06-30


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Be sure to consult your doctor before taking any medication!
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