WELL AT WALGREENS STERILE LUBRICANT EYE- carboxymethylcellulose sodium solution/ drops

Well at Walgreens Sterile Lubricant Eye by

Drug Labeling and Warnings

Well at Walgreens Sterile Lubricant Eye by is a Otc medication manufactured, distributed, or labeled by Walgreens 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

• 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 epain, 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 right away.
• Retain carton for future reference

INDICATIONS & USAGE

Directions

• Put 1 to 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

Benzalkonium chloride solution, boric acid, calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, sodium borate, sodium chloride, sodium hydroxide, sterile purified water

DOSAGE & ADMINISTRATION

Distributed by:

Walgreen Co.

200 Wilmot Rd.

Deerfield, IL 60015

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WELL AT WALGREENS STERILE LUBRICANT EYE 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-7281
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
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-7281-15	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	07/20/2015

Labeler - Walgreens Company (008965063)