GOODSENSE ADVANCED RELIEF EYE- dextran 70, polyethylene glycol 400, povidone, and tetrahydrozoline hci solution/ drops

GoodSense Advanced Relief Eye by

Drug Labeling and Warnings

GoodSense Advanced Relief Eye by is a Otc medication manufactured, distributed, or labeled by Geiss, Destin & Dunn, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients                                             Purpose

Dextran 70 0.1%..............................................Lubricant

Polyethylene glycrol 400 1%..............................Lubricant

Povidone 1%....................................................Lubricant

Tetrahydrozoline HCI 0.05%..............................Redness reliever

PURPOSE

Uses

• for the relief of redness of the eye due to minor eye irritations
• for use as a protectant against further irritation or to relieve dryness of the eye

WARNINGS

Warnings

For external use only

ASK DOCTOR

Ask a doctor before use if you have narrow angle glaucoma.

WHEN USING

When using this product

• pupils may become enlarged temporarily
• overuse may cause more eye redness
• remove contact lenses before using
• do not use if this solution changes color or becomes cloudy
• 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 lasts
• condition worsens or lasts more than 72 hours

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

Directions

• to open bottle, push cap down and twist counter-clockwise. To close bottle, twist clockwise until it stops turning.
• put 1 to 2 drops in the affected eye(s) up to 4 times daily
• children under 6 years of age: ask a doctor

STORAGE AND HANDLING

Other information

• store at 15° to 25°C (59° to 77°F)

INACTIVE INGREDIENT

Inactive ingredients

benzalkonium chloride, boric acid, edetate disodium, purified water, sodium borate, sodium chloride

DOSAGE & ADMINISTRATION

Distributed by:

Geiss, Destin & Dunn, Inc.

Peachtree, City GA 30269

www.valuelabels.com

1-866-696-0957

Made in Korea

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOODSENSE ADVANCED RELIEF EYE 
dextran 70, polyethylene glycol 400, povidone, and tetrahydrozoline hci solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50804-019
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68)	DEXTRAN 70	1 mg  in 1 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	10 mg  in 1 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E)	POVIDONE	10 mg  in 1 mL
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077)	TETRAHYDROZOLINE HYDROCHLORIDE	0.5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
BORIC ACID (UNII: R57ZHV85D4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50804-019-05	1 in 1 BOX	03/24/2016
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	03/24/2016

Labeler - Geiss, Destin & Dunn, Inc. (076059836)