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

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Artificial Tears

Cardinal Health
Bausch & Lomb Incorporated

Artificial Tears Solution Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Polyvinyl Alcohol 1.4%

Purpose

Lubricant

Artificial Tears Uses

  • temporary relieve of burning and irritation due to dryness of the eye

Warnings

  • Do not use if solution changes color or becomes cloudy

 

When using this product  

  • do not touch tip of container to any surface to avoid contamination

Stop use and ask a doctor if

  • you experience eye pain, changes in vision, continued redness or irritation of the eye
  • condition worsens or persists for more than 72 hours

If swallowed, get medical help or contact a Poison Control Center right away

Directions

  • instill 1 to 2 drops in the affected eye(s) as needed

Artificial Tears Other information

  • store at 15° - 30°C (59° - 86°F)
  • keep tightly closed
  • replace cap after use

 

Inactive ingredients

dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate,

purified water, sodium chloride. Phosphoric acid and/or sodium hydroxide may be added to adjust pH. PRESERVATIVE ADDED: benzalkonium chloride 0.01%

Questions ?

Serious side effects associated with use of this product may be reported to 1800-323-0000

DO NOT USE IF IMPRINTED "Protective Seal" WITH YELLOW IS NOT INTACT.

Package/Label Principal Display Panel

Artificial Tears

NDC 37205-137-05

LEADER®

Compare to Liquifilm Tears®* active ingredient*

Artificial Tears Solution

Polyvinyl Alcohol 1.4%

Lubricant Eye Drops

(Sterile)

FOR USE IN THE EYES ONLY

SATISFACTION GUARANTEED 1/2 FL. OZ. (15 mL)

Artificial Tears

Polyvinyl Alcohol SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37205-137
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
POLYVINYL ALCOHOL 14 mg

Inactive Ingredients

Ingredient Name Strength
SODIUM PHOSPHATE, DIBASIC
EDETATE DISODIUM
sodium phosphate, monobasic
SODIUM CHLORIDE
water
benzalkonium chloride

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37205-137-05 15 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-11-15


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