QUALITY CHOICE LUBRICATING EYE DROPS- carboxymethylcellulose sodium, glycerin solution

QUALITY CHOICE LUBRICATING EYE DROPS by

Drug Labeling and Warnings

QUALITY CHOICE LUBRICATING EYE DROPS by is a Otc medication manufactured, distributed, or labeled by CHAIN DRUG MARKETING ASSOCIATION 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 and discomfort due to dryness of the eye or from irritation from wind or sun.

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.

STORAGE AND HANDLING

Other information

• some users may experience a brief tingling sensation
• Store at room temperature.
  

INACTIVE INGREDIENT

Inactive ingredients:

Boric Acid, Sodium Borate, Levocarnitin, Potassium Chloride, Calcium Chloride Dihydrate, Magnesium Chloride, Erythritol, Sodium Citrate Dihydrate, Potassium Sorbate, Purified Water

DOSAGE & ADMINISTRATION

Distributed by C.D.M.A., Inc.

43157 W. Nine Mile

Novi, MI 48376-0995

www.qualitychoice.com

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

QUALITY CHOICE LUBRICATING EYE DROPS 
carboxymethylcellulose sodium, glycerin solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-969
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
BORIC ACID (UNII: R57ZHV85D4)
SODIUM BORATE (UNII: 91MBZ8H3QO)
LEVOCARNITINE (UNII: 0G389FZZ9M)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
ERYTHRITOL (UNII: RA96B954X6)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-969-15	1 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 - CHAIN DRUG MARKETING ASSOCIATION INC (011920774)