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

Walgreens Lubricant Eye Drops by

Drug Labeling and Warnings

Walgreens Lubricant Eye Drops by is a Otc medication manufactured, distributed, or labeled by Walgreen Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                                                                 Purpose

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

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

PURPOSE

Use

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

WARNINGS

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

When using this product

• do not touch tip of container to any surface to avoid contamination
• do not reuse
• once opended, discard

STOP 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, persists or lasts more than 72 hours

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

• Instill 1 or 2 drops in the affected eye(s) as needed.

STORAGE AND HANDLING

Other information

• Store at room temperature

INACTIVE INGREDIENT

Inactive Ingredients

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

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:

WALGREEN CO.

200 WILMOT RD.,

DEERFIELD, IL 60015

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-7220
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	0.4 mg  in 100 mg
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.3 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-7220-25	1 in 1 CARTON
1		25 mg in 1 VIAL, SINGLE-USE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	08/06/2014

Labeler - Walgreen Company (008965063)