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

Extreme Relief Lubricant by

Drug Labeling and Warnings

Extreme Relief Lubricant by is a Otc medication manufactured, distributed, or labeled by Target Corporation. 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 temporary relief of burning and irritation due to eye dryness

WARNINGS

Warnings

For external use only

retain carton for full drug facts

DO NOT USE

Do not use

• if solution changes color or becomes cloudy
• if you are sensitive 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 feel eye pain
• changes in vision occur
• redness or irritation of the eye(s) gets worse, persists or last more than 72 hours

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

• Shake well before use
• Instill 1 or 2 drops in the affected eye(s) as needed

STORAGE AND HANDLING

Other information

• Store at room temperature

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

DISTRIBUTED BY:

TARGET CORP.

MINNEAPOLIS, MN 55403

MADE IN KOREA

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-576
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 CHLORATE (UNII: M536P01U3N)
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: 11673-576-15	1 in 1 BOX
1		15 mL in 1 BOTTLE, DROPPER
2	NDC: 11673-576-30	2 in 1 BOX
2		15 mL in 1 BOTTLE, DROPPER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	03/04/2015

Labeler - Target Corporation (006961700)