GOODSENSE EYE DROPS ADVANCED RELIEF MOISTURIZER- dextran, polyethylene glycol 400, povidone, tetrahydrozoline hcl solution 
Preferred PHarmaceuticals Inc.

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GoodSense Eye Drops Advanced Relief Moisturizer (PLD)

Active Ingredients

Dextran 70.....0.1%

Polyethylene glycol 400.....1%

Povidone.....1%

tetrahydrozoline HCl.....0.05%

Purposes

Dextran 70.....Lubricant

Polyethylene glycol 400.....Lubricant

Povidone.....Lubricant

Tetrahydrozoline HCl .....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 use if you have narrow angle glaucoma

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

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 changed color or becomes cloudy, do not use
•
overuse may produce increased redness of the eye
•
remove contact lens before using

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison control Center (1-800-111-1222) right away.

Directions

Instill 1 to 2 drops in the affected eye(s) up to 4 times daily.

Relabeled By: Preferred Pharmaceuticals Inc.

NDC 68788-8635-1

Inactive ingredients

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

A yellow rectangular object with black text Description automatically generated
GOODSENSE EYE DROPS ADVANCED RELIEF MOISTURIZER 
dextran, polyethylene glycol 400, povidone, tetrahydrozoline hcl solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-8635(NDC:50804-130)
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ) POLYETHYLENE GLYCOL 4001 g  in 100 mL
TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE0.05 g  in 100 mL
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED1 g  in 100 mL
DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 700.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
BORIC ACID (UNII: R57ZHV85D4)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68788-8635-11 in 1 CARTON04/16/2024
115 mL in 1 CARTON; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01804/16/2024
Labeler - Preferred PHarmaceuticals Inc. (791119022)
Registrant - Preferred PHarmaceuticals Inc. (791119022)
Establishment
NameAddressID/FEIBusiness Operations
Preferred PHarmaceuticals Inc.791119022RELABEL(68788-8635)

Revised: 4/2024
Document Id: 011473a8-26d5-4661-b3c0-745f9b6aa1d8
Set id: 011473a8-26d5-4661-b3c0-745f9b6aa1d8
Version: 1
Effective Time: 20240416
 
Preferred PHarmaceuticals Inc.