QUALITY CHOICE LUBRICANT EYE- polyethylene glycol 400, propylene glycol solution/ drops

QUALITY CHOICE LUBRICANT EYE by

Drug Labeling and Warnings

QUALITY CHOICE LUBRICANT EYE 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

Polyethylene Glycol 400 (0.4%)..................................Lubricant

Propylene Glycol (0.3%).............................................Lubricant

PURPOSE

Uses

For the relief of burning, irritation due to dryness of the eye.

WARNINGS

Warnings

For external use only.

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

• to avoid contamination, do not touch tip of container to any surface
• 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

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

INACTIVE INGREDIENT

Inactive ingredients: Boric Acid, Calcium Chloride, Chlorhexidine Gluconate, Hydrochloric Acid, Hydroxypropyl Guar,

Magnesium Chloride, Potassium Chloride, Purified Water, Sodium Chloride, Zinc Chloride

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 LUBRICANT EYE  
polyethylene glycol 400, propylene glycol solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-968
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	4 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3)	PROPYLENE GLYCOL	3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
HYDROCHLORIC ACID (UNII: QTT17582CB)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
POTASSIUM CHLORIDE (UNII: 660YQ98I10)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ZINC CHLORIDE (UNII: 86Q357L16B)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-968-15	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)