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Drug Description

Genadur
(hydrosoluble nail lacquer)
For Topical Use Only

DESCRIPTION

Genadur is a hydrosoluble nail lacquer.

Ingredients

Diethylene glycol monoethylether, equisetum arvense extract, ethanol, hydroxypropyl chitosan, methyl sulfonyl methane, water.

Indications & Dosage

INDICATIONS

Genadur is indicated to protect intact or damaged nails from the effects of moisture, friction (rubbing) or shear (tearing), relieving symptoms and signs of nail dystrophy (i.e. nail splitting and fragility).

DOSAGE AND ADMINISTRATION

Directions

Apply Genadur once daily to clean and dry nails. Using the supplied brush, apply a thin layer of the product on the affected nail(s). Close bottle immediately after use. The film is hydrosoluble, therefore Genadur should be applied after nail washing and drying, preferably before bedtime. Genadur may also be used under a cosmetic colored nail polish, thus protecting the nails from the damaging action of solvents used for polish removal.

HOW SUPPLIED

Genadur Hydrosoluble Nail Lacquer is available in a 12 mL bottle with applicator brush, 43538-510-12.

Store at 15°C to 30°C (59°F to 86°F). Protect from heat.

Mfd. for: Medimetriks Pharmaceuticals, Inc., 383 Route 46 West, Fairfield, NJ 07004-2402 USA. Mfd. by: Polichem S.A., Via Senago 42D, 6912, Lugano-Pazzallo, Switzerland Made in Italy. Revised: Feb 2016

SLIDESHOW

Skin & Beauty: Anti-Aging Tips & Secrets to Look Younger See Slideshow
Side Effects & Drug Interactions

SIDE EFFECTS

No information provided.

DRUG INTERACTIONS

No information provided.

Warnings & Precautions

WARNINGS

Do not use on open wounds. Do not ingest.

FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

PRECAUTIONS

No information provided.

Overdosage & Contraindications

OVERDOSE

No information provided.

CONTRAINDICATIONS

Genadur is contraindicated in persons with known hypersensitivity to any components of the formulation.

Clinical Pharmacology

CLINICAL PHARMACOLOGY

No information provided.

Medication Guide

PATIENT INFORMATION

No information provided. Please refer to the WARNINGS and PRECAUTIONS sections.

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