WALGREENS COMPLETE LUBRICANT EYE DROPS- propylene glycol solution/ drops

Walgreens Complete Lubricant Eye Drops by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

• Active Ingredients: Purpose
• Propylene Glycol 0.6%: Lubricant

Uses

• For relief of dryness of the eye, and protectant against further irritation of the eye.

For temporary relief of burning, irritation, and discomfort including exposure to wind or sun.

Warnings

For use in eyes only.

For external use only.

Retain outer carton for full product drug facts

Do not use

• If solution changes color or becomes cloudy, do not use

When using this product

• To avoid contamination, do not touch tip of container to any surface. Close cap after using

Stop use and ask a doctor if:

• You experience eye pain, changes in vision, continued redness or irritation of the eye.
• The condition worsens or persists for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Shake well.
Wash your hands.
Instill 1 or 2 drops in the affected eye(s) as needed

Other Information

• Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible.
• Use before expiration date marked on container.
• Discard 30 days after opening.
• Store at 59°-86° F (15°-30°C).

Inactive Ingredients

Highly purified water, Boric acid, Hypromellose, Sodium borate, Sodium chloride, Calcium chloride, Benzalkonium chloride, Potassium chloride, Disodium edetate, Magnesium chloride, HCl to adjust pH.

Questions?

1-800-925-4733
9 am to 5 pm EST;
Monday - Friday

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS COMPLETE LUBRICANT EYE DROPS 
propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-2111
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	0.06 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM BORATE (UNII: 91MBZ8H3QO)
BORIC ACID (UNII: R57ZHV85D4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
HYDROCHLORIC ACID (UNII: QTT17582CB)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C16) (UNII: F5UM2KM3W7)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-2111-15	2 in 1 CARTON	03/01/2023
1		10 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	03/01/2023

Labeler - Walgreens (008965063)