WALGREENS LUBRICANT EYE- carboxymethylcellulose sodium solution

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 ingredient                                                                     Purpose

Carboxymethylcellulose Sodium 0.5%......................................Lubricant

PURPOSE

Uses

• For the temporary relief of burning and discomfort due to dryness of the eye or exposure to wind or sun
• May be used as a protectant against further irritation
  

WARNINGS

Warnings

For external use only

DO NOT USE

To avoid contamination, do not touch tip of container to any surface

Replace cap after using.  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 of the eye, or if the 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 immediately
• Retain carton for future reference.
  

INDICATIONS & USAGE

Directions

• Put 1 or 2 drops in the affected eye/s as needed
  

STORAGE AND HANDLING

Other information

• store at room temperature 15o to 30oC (59o to 86oF)
  

INACTIVE INGREDIENT

Boric Acid, Calcium Chloride, Magnesium Chloride, Potassium Chloride, Sterile Purified Water, Benzalkonium Chloride, Sodium Borate, Sodium Chloride

DOSAGE & ADMINISTRATION

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

walgreens.com

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WALGREENS LUBRICANT EYE  
carboxymethylcellulose sodium solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-1466
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-1466-30	2 in 1 CARTON
1		15 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	09/30/2012

Labeler - WALGREEN COMPANY (008965063)