Product Images Flarex

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Product Label Images

The following 5 images provide visual information about the product associated with Flarex NDC 71776-100 by Eyevance Pharmaceuticals, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

FLAREX Sample Carton

FLAREX Sample Carton

This is a pharmaceutical product for topical ophthalmic use only. It contains Activ fluorometholone acetate 0.1 and benzalkonium chloride 0.01%. The product should be stored upright between 2 to 25°C and protected from freezing. The recommended dosage is one to two drops into the conjunctival sacs four times daily, and it can be increased to two drops every two hours within the first 24 to 48 hours. If there is no improvement after two weeks, a physician should be consulted. Discontinuing the therapy prematurely should be avoided. The product is manufactured by Eyevance Pharmaceuticals, LLC in Italy, and it's not available for sale as it's a sample.*

FLAREX Sample Label

FLAREX Sample Label

This is a prescription-only medication called Fluorometholone acetate, which is sterile and intended for topical use in the eyes. It contains 0.1% (1 mg) of the active ingredient Fluorometholone acetate and benzalkonium chloride 0.01% as a preservative. Before use, shake the bottle well. Recommended dosage is one to two drops in each eye's conjunctival sac, four times per day, which can be increased to two drops every two hours safely over the first 24 to 48 hours if required. If there is no improvement after 10 weeks of use, consult a physician. This medication should not be discontinued prematurely. Store this medication upright between 2°C -25°C (36°F -77°F) and protect it from freezing.*

image description 2 - Flarex Box Label

image description 2 - Flarex Box Label

Flarex (fluorometholone acetate ophthalmic suspension) 0.1% is a prescription medication used to treat inflammation of the eye. It should be stored upright between 2°C and 25°C, protected from freezing. Each mL contains fluorometholone acetate 0.1% as an active ingredient, with benzalkonium chloride 0.01% as a preservative, and other inactive ingredients. The recommended dosage is one to two drops in the conjunctival sac(s) four times daily, with a possible increase in dosage within the first 24-48 hours. Premature discontinuation of treatment should be avoided, and any improvement after two weeks should be discussed with a physician. Flarex is produced by Eyevance Pharmaceuticals in Italy.*

image description 1 - Flarex Container Label

image description 1 - Flarex Container Label

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* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.