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

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FREDS DRY EYE RELIEF

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

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients                                                                Purpose

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

Polyethylene Glycol 400 1% ...............................................Lubricant

Hypromellose 0.2% ............................................................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 if this solution changes 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
  • condition worsens 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

  • put 1 to 2 drops in the affected eye(s) up to 4 times daily
  • children under 6 years of age: ask a doctor

Other information

  • some users may experience a brief tingling sensation
  • store at 15o to 25oC (59o to 77oF)

Inactive ingredients: ascorbic acid, benzalkonium chloride, boric acid, dextrose, disodium phosphate, glycine, magnesium chloride, potassium chloride, purified water,

sodium borate, sodium chloride, sodium citrate, and sodium lactate

Distributed by: Fred's Inc.

                      4300 New Getwell Rd.

                      Memphis, TN 38118


www.fredsinc.com

FREDS DRY EYE RELIEFEnter section text here

FREDS DRY EYE RELIEF

GLYCERIN SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11716-1189
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

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

Inactive Ingredients

Ingredient Name Strength
ASCORBIC ACID
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:11716-1189-9 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-12-06


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Be sure to consult your doctor before taking any medication!
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