CVS LONG LASTING LUBRICANT EYE- polyethylene glycol 400 and propylene glycol solution/ drops 
CVS Pharmacy, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients                                                                 Purpose

Polyethylene Glycol 400 0.4%                                                 Lubricant

Propylene Glycol 0.3%                                                            Lubricant

Uses

For the temporary relief of burning and irritation due to eye dryness.

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

Keep out of the reach of children

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

Directions

Other information

Inactive ingredients boric acid, calcium chloride, chlorhexidine gluconate, hydrochloric acid, hypromellose 2910, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, zinc chloride

Distributed By:

CVS Pharmacy, Inc.

One CVS Drive

Woonsocket, RI 02895

Made in Korea

image description

CVS LONG LASTING LUBRICANT EYE 
polyethylene glycol 400 solution/ drops
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-151
Route of Administration OPHTHALMIC DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 400 0.4 mg  in 1 mg
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 0.3 mg  in 1 mg
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)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ZINC CHLORIDE (UNII: 86Q357L16B)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:59779-151-15 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 09/17/2013
Labeler - CVS Pharmacy, Inc. (062312574)

Revised: 9/2013
Document Id: c5122649-b40b-4876-8eed-7ba624765226
Set id: 15d2f06f-9c4f-4025-975e-336f29ed2a5d
Version: 1
Effective Time: 20130917
 
CVS Pharmacy, Inc.