EQUATE LUBRICATING EYE- carboxymethylcellulose sodium, and glycerin solution/ drops

EQUATE LUBRICATING EYE by

Drug Labeling and Warnings

EQUATE LUBRICATING EYE by is a Otc medication manufactured, distributed, or labeled by WAL-MART STORES INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients                                                              Purpose

Carboxymethylcellulose Sodium 0.5%------------------------- Lubricant

Glycerin 0.9%--------------------------------------------------- Lubricant

PURPOSE

Uses

• For the temporary relief of burning, irritation 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

retain carton for full product drug facts

DO NOT USE

Do not use

• if solution changes color or becomes cloudy
• if you are sensitive or allergic to any ingredient in this product

WHEN USING

When using this product

• do not touch tip of container to any surface to avoid contamination
• replace cap after each use

STOP USE

Stop use and ask a doctor if

• you experience eye pain
• changes in vision occur
• redness or irritation of the eye(s) gets worse or lasts 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.

STORAGE AND HANDLING

Other information

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

INACTIVE INGREDIENT

Inactive ingredients

benzalkonium chloride, boric acid, calcium chloride dihydrate, erythritol, levocarnitine, magnesium chloride, potassium chloride, purified water, sodium borate, sodium citrate dihydrate

DOSAGE & ADMINISTRATION

Distributed by:

Wal-Mart Stores, Inc.,

Bentonville, AR 72716

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EQUATE LUBRICATING EYE 
carboxymethylcellulose sodium, and glycerin solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-936
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
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	9 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORATE DIHYDRATE (UNII: BBB2RG413E)
ERYTHRITOL (UNII: RA96B954X6)
LEVOCARNITINE (UNII: 0G389FZZ9M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-936-15	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	04/01/2012

Labeler - WAL-MART STORES INC. (051957769)