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

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LiquiTears

H.J. Harkins Company, Inc.
Bausch & Lomb Incorporated

Artificial Tears Solution Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Polyvinyl Alcohol 1.4%

Purpose

Lubricant

LiquiTears Uses

  • to prevent further irritation
  • to relieve 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
  • replace cap after use

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

LiquiTears Other information

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

 

Inactive ingredients

dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate, sodium chloride,

purified water. 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

*MAJOR LIQUITEARS IS NOT MANUFACTURED OR DISTRIBUTED BY ALLERGAN, INC. OWNER OF THE REGISTERED TRADEMARK, LIQUIFILM TEARS®.

Package/Label Principal Display Panel

LiquiTears

MAJOR®

NDC 0904-5017-35

LiquiTears

Polyvinyl Alcohol 1.4%

Lubricant Eye Drops (Sterile)

Relieves Burning due to Dryness of the Eye

Compare to Active Ingredient of Liquifilm Tears®*

1/2 FL. OZ. (15 mL)

Repacked by:
H.J. Harkins Company, Inc.
Grover Beach, CA 93433

LiquiTears

Polyvinyl Alcohol SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52959-041(NDC:0904-5017)
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:52959-041-00 15 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2011-12-09


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