Label: GOODSENSE EYE DROPS ADVANCED RELIEF MOISTURIZER- dextran, polyethylene glycol 400, povidone, tetrahydrozoline hcl solution
- NDC Code(s): 68788-8635-1
- Packager: Preferred PHarmaceuticals Inc.
- This is a repackaged label.
- Source NDC Code(s): 50804-130
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 16, 2024
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only
Stop use and ask a doctor if you experience
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- eye pain
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- changes in vision
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- continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours
When using this product
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- pupils may become enlarged temporarily
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- to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
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- if solution changed color or becomes cloudy, do not use
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- overuse may produce increased redness of the eye
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- remove contact lens before using
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GOODSENSE EYE DROPS ADVANCED RELIEF MOISTURIZER
dextran, polyethylene glycol 400, povidone, tetrahydrozoline hcl solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68788-8635(NDC:50804-130) 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 1 g in 100 mL TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.05 g in 100 mL POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) (POVIDONE - UNII:FZ989GH94E) POVIDONE, UNSPECIFIED 1 g in 100 mL DEXTRAN 70 (UNII: 7SA290YK68) (DEXTRAN 70 - UNII:7SA290YK68) DEXTRAN 70 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:68788-8635-1 1 in 1 CARTON 04/16/2024 1 15 mL in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 04/16/2024 Labeler - Preferred PHarmaceuticals Inc. (791119022) Registrant - Preferred PHarmaceuticals Inc. (791119022) Establishment Name Address ID/FEI Business Operations Preferred PHarmaceuticals Inc. 791119022 RELABEL(68788-8635)