GoodSense Eye Drops Advanced Relief Moisturizer

DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL OPHTHALMIC HUMAN OTC DRUG

GoodSense Eye Drops Advanced Relief Moisturizer is an FDA drug label for the active ingredient DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL manufactured by Preferred PHarmaceuticals Inc. administered by OPHTHALMIC. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260429.

Generic name
DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL
Manufacturer
Preferred PHarmaceuticals Inc.
Product type
HUMAN OTC DRUG
Route
OPHTHALMIC
Dosage form
N/A
NDC
68788-8635
Application
M018
Label effective
20260429

About this product

GoodSense Eye Drops Advanced Relief Moisturizer is an FDA-registered drug product whose active ingredient is DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL. It is labelled by Preferred PHarmaceuticals Inc. taken by ophthalmic and marketed as a human otc drug product. Identifiers on file: NDC 68788-8635, application M018, label effective 20260429. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL are most often described in connection with: relieves redness, eye due, irritations lubricant, irritation relieve. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients Dextran 70.....0.1% Polyethylene glycol 400.....1% Povidone.....1% tetrahydrozoline HCl.....0.05%

Indications & Usage

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

Dosage & Administration

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

Warnings

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.

Frequently asked questions

What is GoodSense Eye Drops Advanced Relief Moisturizer used for?
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

Who makes GoodSense Eye Drops Advanced Relief Moisturizer?
Preferred PHarmaceuticals Inc. is the labeler of record for GoodSense Eye Drops Advanced Relief Moisturizer.

What form does GoodSense Eye Drops Advanced Relief Moisturizer come in?
administered by ophthalmic. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is GoodSense Eye Drops Advanced Relief Moisturizer prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has GoodSense Eye Drops Advanced Relief Moisturizer been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.