GOOD NEIGHBOR PHARMACY LUBRICANT EYE DROPS description, usages, side effects, indications, overdosage, supplying and lots more!

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GOOD NEIGHBOR PHARMACY LUBRICANT EYE DROPS

HANLIM PHARM. CO., LTD.
UNITED EXCHANGE CORP.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients                                                                   Purpose

Polyethylene Glycol 400 (0.4%) ..............................................Lubricant

Propylene Glycol (0.3%) .........................................................Lubricant

Purpose

Uses

  • For the temporary relief of burning and irritation due to dryness of the eyes.
  • For protection against further irritation.

Warnings

For external use only.

Do not use

  • if this product changes color or becomes cloudy.
  • if you are sensitive to any ingredient in this product.

When using this product

  • Do not touch tip of container to 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(s) gets worse or lasts 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

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

Other information

  • Store at room temperature
  • Do not use if carton is open or neckband on the bottle is broken or missing

Inactive ingredients: Boric Acid, Calcium Chloride, Chlorhexidine Gluconate, Hydrochloric Acid, Hypromellose 2910, Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Chloride, Sodium Hydroxide, Zinc Chloride

Distributed by:

AmerisourceBergen Corporation

1300 Morris Drive

Chesterbrook, PA 19087


Side effects occur.

You may report side effects to FDA at 1-800-FDA-1088.


GOOD NEIGHBOR PHARMACY LUBRICANT EYE DROPSEnter section text here

GOOD NEIGHBOR PHARMACY LUBRICANT EYE DROPS

POLYETHYLENE GLYCOL 400 SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11716-4060
Route of Administration OPHTHALMIC DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
polyethylene glycol 400 Polyethylene Glycol 400 0.4 mL
propylene glycol Propylene Glycol 0.3 mL

Inactive Ingredients

Ingredient Name Strength
BORIC ACID
calcium chloride
chlorhexidine gluconate
HYDROCHLORIC ACID
HYPROMELLOSE 2910 (4000 CPS)
MAGNESIUM CHLORIDE
potassium chloride
water
SODIUM CHLORIDE
SODIUM HYDROXIDE
ZINC CHLORIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 15 in 1 BOTTLE
2 NDC:11716-4060-9 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part349 2010-09-20


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Be sure to consult your doctor before taking any medication!
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