WALGREENS LUBRICANT EYE- sodium carboxymethylcellulose 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

Sodium carboxymethycellulose 0.25%..................................Lubricant

PURPOSE

Uses

• As a lubricant to relieve dryness of the eye
• As a protectant against further irritation of the eye
• For temporary relief of burning, irritation, and discomfort including exposure to wind or sun

WARNINGS

Warnings

For external use only

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

DO NOT USE

Do not use

• if solution changes color or becomes cloudy.

STOP USE

Stop use and ask a doctor if

• you experience eye pain, changes in vision, continued redness or irritation
• condition worsens or persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children.

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

benzalkonium chloride, boric acid, calcium chloride, magnesium chloride, potassium chloride, sodium bicarbonate, sodium borate, sodium chloride, sodium dihydrogen phosphate monohydrate, water

DOSAGE & ADMINISTRATION

Distributed by:

Walgreen Co.

200 Wilmont Rd.

Deerfield, IL 60015

Made in South Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS LUBRICANT EYE 
sodium carboxymethylcellulose solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0084
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	2.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
WATER (UNII: 059QF0KO0R)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0084-15	1 in 1 BOX	06/04/2018
1		15 mL in 1 BOTTLE; 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	06/04/2018

Labeler - Walgreen Company (008965063)