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Drug Uses

Penlac is an antifungal indicated as topical treatment for onychomycosis of fingernails and toenails.

How Taken

Before you start applying Penlac, remove any loose nail or nail material using nail clippers or nail files. Apply Penlac once daily (preferably at bedtime) to all affected nails with the applicator brush provided. Apply the lacquer evenly over the entire nail. Allow the lacquer to dry (approximately 30 seconds) before putting on socks or stockings. After applying this medication, wait 8 hours before taking a bath or shower.

Warnings/Precautions

Use Penlac only on nails and immediately adjacent skin. Avoid contact with the eyes and mouth.

Missed Dose

Apply Penlac as soon as you remember.

Possible Side Effects

The most common adverse reactions are rash-related. Inform your health care professional if the area of application shows signs of increased irritation (redness, itching, burning, blistering, swelling, oozing)

Storage

Store Penlac at room temperature between 59° and 86° F (15° and 30° C). Keep out of the reach of children.

Overdose

Overdoses are highly unlikely to occur. Seek medical attention if you suspect an overdose.

More Information

Do not use nail polish or other nail cosmetic products on the treated nails. Avoid use near heat or open flame, because product is flammable.

Disclaimer

This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information, including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.

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Before taking Ultracet, tell your doctor if you also use: carbamazepine (Tegretol); warfarin (Coumadin); digoxin (Lanoxin, Lanoxicaps); ketoconazole (Nizoral); erythromycin (E-Mycin, E.E.S., Ery-Tab); rifampin (Rifadin, Rimactane, Rifater); St. John's wort; quinidine (Quinaglute, Quinidex, Cardioquin, Quinora); or an antidepressant such as amitriptyline (Elavil), citalopram (Celexa), clomipramine (Anafranil), desipramine (Norpramin), escitalopram (Lexapro), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), imipramine
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F.A.Q

Q. What is your policy on medication expiry dates for Penlac?
Ultracetrx.com fully complies with all the policies in expiry dates.
We always dispense the best dated products available. Generally our products will have an expiry date of at least one to two years from when we dispense them. In fact, we remove medication from our shelves at least four months prior to the date they expire.

What are the differences between Penlac brand-name drugs and Penlac generic drugs?
You probably know that pharmaceutical companies carry out extensive research and clinical testing to win approval from the Food and Drug Administration for new drugs. The new drug is then protected by patent for at least 10 years. Hence, a brand-name drug. When the patent expires another drug company can "copy the recipe" for the brand drug. This "copy" is called a generic drug. The FDA requires that generic Penlac have the same active chemical composition, be dispensed in the same dosage form such as a tablet or capsule and be taken in the same dosage as the brand-name drug.
Ultracetrx.com recommends the use of a generic drug only when it is "A" rated, the highest bioequivalent rating by the FDA.

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Different definition / meanings for the word "Anxiety disorders":
Conditions in which anxiety disrupts ordinary functioning or causes significant distress to the sufferer. “Anxiety” refers to one’s response to any perceived threat of danger (real or imagined), and includes physical (such as increased heart rate and shortness of breath), mental (attention drawn to the perceived threat), and behavioral (avoidance or escape) components.

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An application to the FDA asking for approval to market a new drug.

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