EXTREME RELIEF LUBRICANT- polyethylene glycol 400, and propylene glycol solution/ drops 
Target Corporation

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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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

retain carton for full drug facts

Do not use

When using this product

Stop use and ask a doctor if

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

Other information

Inactive ingredients

boric acid, calcium chloride, 20% chlorhexidine, glyconate, hydrochloric acid, hypromellose 2910, magnesium chloride, potassium chloride, purified water, sodium chloride, sodium hydroxide, zinc chloride

DISTRIBUTED BY:

TARGET CORP.

MINNEAPOLIS, MN 55403

MADE IN KOREA

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EXTREME RELIEF LUBRICANT 
polyethylene glycol 400, and propylene glycol solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-576
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4004 mg  in 1 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID (UNII: R57ZHV85D4)  
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)  
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
MAGNESIUM CHLORATE (UNII: M536P01U3N)  
POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ZINC CHLORIDE (UNII: 86Q357L16B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-576-151 in 1 BOX
115 mL in 1 BOTTLE, DROPPER
2NDC:11673-576-302 in 1 BOX
215 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34903/04/2015
Labeler - Target Corporation (006961700)

Revised: 3/2015
Document Id: 78468987-8704-4cf7-aacc-9be173e99241
Set id: 6fe0e844-268e-42d7-bc98-57b4f001911b
Version: 1
Effective Time: 20150304
 
Target Corporation