WALGREENS LUBRICANT EYE DROPS- polyethylen glycol and propylene gloycol solution/ drops 
Walgreen Company

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.

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Active Ingredient                                                                                 Purpose

Polyethylene Glycol 400 0.4%----------------------------------------------- Lubricant

Propylene Glycol 0.3%------------------------------------------------------- Lubricant

Use

Warnings:

For external use only.

Do not use

When using this product

Stop use and ask a doctor if

 Keep out of the reach of chilren.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

Inactive Ingredients

aminomethylpropanol, boric acid, hydrochloric acid, hydroxy ethyl cellulose, potassium chloride, sodium chloride, sodium hydroxide, sorbitol, water for injection

DISTRIBUTED BY:

WALGREEN CO.

200 WILMOT RD.,

DEERFIELD, IL 60015

image description

WALGREENS LUBRICANT EYE DROPS 
polyethylen glycol and propylene gloycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7220
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4000.4 mg  in 100 mg
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL0.3 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
BORIC ACID (UNII: R57ZHV85D4)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SORBITOL (UNII: 506T60A25R)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-7220-251 in 1 CARTON
125 mg in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34908/06/2014
Labeler - Walgreen Company (008965063)

Revised: 8/2014
Document Id: df022a54-279e-4c8c-af91-3c54c7fba69d
Set id: 77a8ae01-61ad-4c40-a493-f98c2d29bf81
Version: 1
Effective Time: 20140806
 
Walgreen Company