CVS MOISTURIZING LUBRICATING EYE- carboxymethylcellulose sodium solution/ drops

CVS Moisturizing Lubricating Eye by

Drug Labeling and Warnings

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

Drug Details [pdf]

Drug Facts

Active Ingredients                                                                     Purpose

Carboxymethylcellulose Sodium 0.5%                                           Lubricant

Glycerin 0.9%                                                                             Lubricant

PURPOSE

Uses

For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or from irritation from wind or sun.

May be used to protect against further irritation

WARNINGS

Warnings

For external use only.

WHEN USING

When using this product

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

Do not use if solution changes color or gets cloudy.

STOP USE

Stop use and ask a doctor if

You feel 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 reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

INDICATIONS & USAGE

Directions

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

Do not use if neck band is broken or missing.

INACTIVE INGREDIENT

Inactive ingredients: Boric Acid, Calcium Chloride Dihydrate, Chlorhexidine Gluconate, Erythritol, Hexahydrate, Levocarnitine, Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Borate Decahydrate, Sodium Citrate Dihydrate

DOSAGE & ADMINISTRATION

Distributed by:

CVS Pharmacy, Inc.

One CVS Drive,

Woonsocket, RI 02895

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CVS MOISTURIZING LUBRICATING EYE 
carboxymethylcellulose sodium solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59779-150
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 100 mg
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	9 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
ERYTHRITOL (UNII: RA96B954X6)
LEVOCARNITINE (UNII: 0G389FZZ9M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59779-150-15	1 in 1 CARTON
1		15 mg in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	09/03/2013

Labeler - CVS Pharmacy (062312574)