Rexall Sterile Artificial Tears Eye Drops description, usages, side effects, indications, overdosage, supplying and lots more!

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Rexall Sterile Artificial Tears Eye Drops

Dolgencorp Inc

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 use
  • do not use if this solution changes color or becomes cloudy
  • do not touch tip of container or 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 last more than 72 hours

If pregnant or breast-feeding, ask a health professional before use.

Keep out of 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) as needed.
  • children under 6 years of age: ask a doctor.

Other information

  • some users may experience a brief tingling sensation
  • store at 15° to 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, sodium lactate.

Packaged For:

Dolgencorp, LLC

100 Mission Ridge

Goodlettsville, TN 37072 USA

Made in Korea

Rexall Sterile Artificial Tears Eye Drops

Rexall Sterile Artificial Tears Eye Drops

Glycerin SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55910-522
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:55910-522-15 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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