Eye Drops Lubricating Tears description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Eye Drops Lubricating Tears

KC Pharmaceuticals, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Glycerin 0.2%

Hypromellose 0.2%

Polyethylene glycol 400 1%

Purpose

Glycerin - Lubricant

Hypromellose - Lubricant

Polyethylene glycol 400 - Lubricant

Keep out of reach of children.

If accidentally swallowed, get medical help or contact a Poison Control Center immediately.

Eye Drops Lubricating Tears 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

  • Do not use this product if solution changes color or becomes cloudy

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

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using.  Keep container tightly closed.
  • remove contact lens before using

Directions

  • Instill 1 or 2 drops in the affected eye(s) as needed.
  • Children under 6 years of age: ask a doctor

Inactive Ingredients

dextrose, sodium chloride, potassium chloride, sodium phosphate monobasic, sodium phosphate dibasic, sodium bicarbonate, sodium citrate, edetate disodium, benzalkonium chloride, purified water

Eye Drops Lubricating Tears Other information

  • Tamper Evident.  Do not use this product if imprinted neckband on bottle is broken or missing.
  • Retain this carton for future reference
  • Store at 15o - 30oC (59o - 86oF)

If pregnant or breast feeding,

ask a health professional before use

Principal Display Panel

EDLT

Eye Drops Lubricating Tears

Eye Drops Lubricating Tears

Hypromellose, Glycerin, Polyethylene glycol 400 SOLUTION/ DROPS

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55651-026
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HYPROMELLOSES 2 mg
GLYCERIN 2 mg
polyethylene glycol 400 Polyethylene Glycol 400 10 mg

Inactive Ingredients

Ingredient Name Strength
benzalkonium chloride
DEXTROSE
EDETATE DISODIUM
potassium chloride
water
SODIUM BICARBONATE
SODIUM CHLORIDE
SODIUM CITRATE
SODIUM PHOSPHATE, DIBASIC ANHYDROUS
Sodium Phosphate, Monobasic, Monohydrate

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE, DROPPER
2 NDC:55651-026-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2008-05-12


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.