GOOD NEIGHBOR PHARMACY EYE DROPS ADVANCED RELIEF- dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hydrochloride solution/ drops

Good Neighbor Pharmacy Eye Drops by

Drug Labeling and Warnings

Good Neighbor Pharmacy Eye Drops by is a Otc medication manufactured, distributed, or labeled by AmerisourceBergen Drug Corporation, K.C. Pharmaceuticals, Inc., KC Pharmaceuticals, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Dextran 70 0.1%

Polyethylene glycol 400 1%

Povidone 1%

Tetrahydrozoline HCl 0.05%

Purpose

Eye lubricant and Redness reliever

Uses

relieves redness of the eye due to minor eye irritations

as a lubricant to prevent further irritation or to relieve dryness of the eye

Warnings

For external use only

Ask a doctor before us if

you have narrow angle glaucoma

when using this product

pupils may become enlarged temporarily

to avoid contamination, do not touch tip of container to any surface. Replace cap after using.

if solution changes color or becomes cloudy,do not use

overuse may produce increased redness of the eye

remove contact lens before using

stop use and ask a doctor if

you experience eye pain

changes in vision

continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours

If pregnant or breastfeeding

ask a health professional before use.

Keep out of reach of children

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

Directions

Instill 1 or 2 drops in the affected eye(s) up to four times daily

Other information

Store at 15 °-30°C (59°-86°F)

Inactive ingredients

benzalkonium chloride,

boric acid, edetate

disodium, purified

water, sodium borate,

and sodium chloride

Good Neighbor Pharmacy Eye Drops

INGREDIENTS AND APPEARANCE

GOOD NEIGHBOR PHARMACY EYE DROPS  ADVANCED RELIEF
dextran 70, polyethylene glycol 400, povidone, tetrahydrozoline hydrochloride solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24385-077
Route of Administration	INTRAOCULAR

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68)	DEXTRAN 70	0.1 g  in 100 mL
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	1 g  in 100 mL
POVIDONE (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E)	POVIDONE	1 g  in 100 mL
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077)	TETRAHYDROZOLINE HYDROCHLORIDE	0.05 g  in 100 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: 24385-077-05	15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	01/29/2001

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part349	01/29/2001

Labeler - AmerisourceBergen Drug Corporation (007914906)

Registrant - K.C. Pharmaceuticals, Inc. (174450460)

Establishment
Name	Address	ID/FEI	Business Operations
KC Pharmaceuticals, Inc		174450460	manufacture(24385-077) , label(24385-077)