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GNP Lubricant Eye

Medically reviewed on June 30, 2017.

Dosage form: solution/ drops
Ingredients: POLYETHYLENE GLYCOL 400 0.4mg in 1mg, PROPYLENE GLYCOL 0.3mg in 1mg
Labeler: Amerisource Bergen
NDC Code: 46122-018

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredients                                                              Purpose

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

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

Uses

  • For the temporary relief of burning and irritation due to dryness of the eye.

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) get 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.

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 Avid, Calcium Chloride, Chlorhexidine Gluconate, Hydrochloric Acid, Hypromellose 2910, Magnesium Chloride, Potassium Chloride, Purified Water, Sodim Chloride, Sodium Hydroxide, Zinc Chloride

Distributed By:

Amerisource Bergen Corporation

1300 Morris Drive

Chesterbrook, PA 19087  

Made in Korea

GNP LUBRICANT EYE  
polyethylene glycol 400 solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-018
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (POLYETHYLENE GLYCOLS) POLYETHYLENE GLYCOL 4000.4 mg  in 1 mg
PROPYLENE GLYCOL (PROPYLENE GLYCOL) PROPYLENE GLYCOL0.3 mg  in 1 mg
Inactive Ingredients
Ingredient NameStrength
BORIC ACID 
CALCIUM CHLORIDE 
CHLORHEXIDINE GLUCONATE 
HYDROCHLORIC ACID 
MAGNESIUM CHLORIDE 
POTASSIUM CHLORIDE 
WATER 
SODIUM CHLORIDE 
SODIUM HYDROXIDE 
ZINC CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:46122-018-051 BOTTLE (BOTTLE) in 1 CARTON
115 mg in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34906/30/2013
Labeler - Amerisource Bergen (007914906)

 
Amerisource Bergen

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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