WALGREENS LUBRICANT EYE- polyethylene glycol 400 and propylene glycol solution/ drops

Walgreens Lubricant Eye by

Drug Labeling and Warnings

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

Drug Details [pdf]

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 eye dryness.

WARNINGS

For external use only

DO NOT USE

Do not use

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

WHEN USING

When using this product

• to avoid contamination, do not touch tip of container to any surface.
• replace cap after each use.

STOP USE

Stop use and ask a doctor if you have 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.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

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

INDICATIONS & USAGE

Directions

• Shake well before use.
• Put 1 or 2 drops in the affected eye(s) as needed.

STORAGE AND HANDLING

Other information

Store at room temperature 15-30°C (59-86°F)

INACTIVE INGREDIENT

Inactive ingredients

boric acid, calcium chloride, chlorhexidine gluconate, hydrochloric acid, hypromellose 2910, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, zinc chloride

DOSAGE & ADMINISTRATION

Distributed by:

Walgreen Co.

200 Wilmot Rd.

Deerfield, IL 60015

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS LUBRICANT EYE 
polyethylene glycol 400 and propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-7267
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	4 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ZINC CHLORIDE (UNII: 86Q357L16B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-7267-15	1 in 1 CARTON
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	07/21/2015

Labeler - Walgreen Company (008965063)