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Medically reviewed by Last updated on Jul 27, 2019.


(pol ee yoor EE a URE e thane)

Index Terms

  • Poly Urea Urethane
  • Polyureaurethane

Dosage Forms

Excipient information presented when available (limited, particularly for generics); consult specific product labeling.

Solution, topical:

Nuvail™: 16% (15 mL)

Brand Names: U.S.

  • Nuvail™

Pharmacologic Category

  • Protectant, Topical


Biocompatible, polymeric solution; forms uniform film that protects nail from abrasion, friction, and moisture

Use: Labeled Indications

Nail dystrophy: Management of signs and symptoms of nail dystrophy such as nail splitting and nail fragility for intact or damaged nails.


Use with deep, open, or profusely bleeding wounds

Dosing: Adult

Nail dystrophy: Topical: Apply once daily before bedtime to affected nail(s)

Dosing: Geriatric

Refer to adult dosing.


Apply evenly to affected nail plate, proximal and lateral folds, and distal tip; allow to dry completely. Clean affected nails with nail polish remover once weekly. Use of other topical products before application of poly-ureaurethane may prevent film formation and reduce effectiveness. To avoid staining, avoid contact with finished surfaces (eg, furniture, counter tops).


Store at 15°C to 30°C (59°F to 86°F); avoid excessive heat and humidity. Flammable liquid; keep away from heat and flame; use in well-ventilated area.

Drug Interactions

There are no known significant interactions.

Adverse Reactions

Frequency not defined: Dermatologic: Skin irritation, stinging of the skin


Concerns related to adverse effects:

• Skin irritation: May sting upon application; discontinue use if redness or other signs of irritation occur.

Special populations:

• Isocyanate sensitization: Patients sensitized to isocyanate should not use poly-ureaurethane.

Other warnings/precautions:

• Flammable: Formulation is flammable; do not expose to high temperatures or near open flame. Use in a well-ventilated area.

Patient Education

• Discuss specific use of drug and side effects with patient as it relates to treatment. (HCAHPS: During this hospital stay, were you given any medicine that you had not taken before? Before giving you any new medicine, how often did hospital staff tell you what the medicine was for? How often did hospital staff describe possible side effects in a way you could understand?)

• Patient may experience stinging. Have patient report immediately to prescriber severe skin irritation.

• Educate patient about signs of a significant reaction (eg, wheezing; chest tightness; fever; itching; bad cough; blue skin color; seizures; or swelling of face, lips, tongue, or throat). Note: This is not a comprehensive list of all side effects. Patient should consult prescriber for additional questions.

Intended Use and Disclaimer: Should not be printed and given to patients. This information is intended to serve as a concise initial reference for health care professionals to use when discussing medications with a patient. You must ultimately rely on your own discretion, experience, and judgment in diagnosing, treating, and advising patients.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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