Walgreen Sterile Lubricant Drops 70 Count description, usages, side effects, indications, overdosage, supplying and lots more!

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Walgreen Sterile Lubricant Drops 70 Count

WALGREEN COMPANY


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Walgreen Sterile Lubricant Single Use Eye Drops 70 Count Drug Facts

Active Ingredients                                              Purpose

Carboxymethylcellulose sodium 0.5%................. Eye lubricant

Purpose

Uses

  • For the temporary relief of buring, irritation, and discomofort due to dryness of the eye or exposure to wind or sun
  • May be used as a protectant against further irritation

Warnings

For external use only

  • To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard
  • Do not touch unit-dose tip to eye
  • If solution changes color or becomes cloudy, do not use

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists 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

To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container

  • if used for post-operative (e.g. LASIK) dryness and discomfort, follow your eye doctor's instructions

Other information

  • Use only if single-use container is intact
  • Use before exipration date marked on container
  • Store at 59°-86°F (15°-30°C)
  • RETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive ingredients

calcium chloride, magnesium chloride, potassium chloride, purified water, sodium chloride, and sodium lactate. May also contain hydrochloric acid and or/sodium hydroxic to adjust pH

DISTRIBUTED BY:

WALGREEN CO.

200 WILMOT ROAD

DEERFIELD, IL 60015 USA

Walgreen Sterile Lubricant Drops 70 Count

Walgreen Sterile Lubricant Drops 70 Count

Carboxymethylcellulose sodium SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0363-4809
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CARBOXYMETHYLCELLULOSE SODIUM 5 mg

Inactive Ingredients

Ingredient Name Strength
calcium chloride
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM CHLORIDE
sodium lactate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 .4 in 1 VIAL, SINGLE-USE
2 NDC:0363-4809-70 70 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2014-03-25


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