CVS LUBRICANT EYE- sodium carboxymethylcellulose solution/ drops

CVS Lubricant Eye by

Drug Labeling and Warnings

CVS Lubricant Eye by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                                             Purpose

Sodium Carboxymethylcellulose 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 occur, continued redness or irritation
• 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

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

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:

CVS Pharmacy, Inc.

One CVS Drive

Woonsocket, RI 02895

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS LUBRICANT EYE 
sodium carboxymethylcellulose solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-755
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)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM PHOSPHATE, MONOBASIC, DIHYDRATE (UNII: 5QWK665956)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-755-30	2 in 1 CARTON	03/04/2016
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	03/04/2016

Labeler - CVS Pharmacy (062312574)