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URE-K

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Overview

What is URE-K?

URE-K 50%

Each gram of cream contains:

ACTIVE:

INACTIVES:



What does URE-K look like?



What are the available doses of URE-K?

Sorry No records found.

What should I talk to my health care provider before I take URE-K?

Sorry No records found

How should I use URE-K?

For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or prurient debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.

Apply cream to affected skin twice per day or as directed by a physician. Rub in until completely absorbed. Apply to diseased or damaged nail tissue twice per day or as directed by a physician.


What interacts with URE-K?

Sorry No Records found


What are the warnings of URE-K?

Sorry No Records found


What are the precautions of URE-K?

Sorry No Records found


What are the side effects of URE-K?

Sorry No records found


What should I look out for while using URE-K?

URE-K 50%

For external use only. Avoid contact with eyes, lips or mucous membranes. Do not use on areas of broken skin.


What might happen if I take too much URE-K?

Sorry No Records found


How should I store and handle URE-K?

URE-K 50%


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Urea gently dissolves the intercellular matrix which results in loosening the horny layer of skin and shedding scaly skin at regular intervals, thereby softening hyperkeratotic areas. Urea also hydrates and gently dissolves the intercellular matrix of the nail plate, which can result in the softening and eventual debridement of the nail plate.

Non-Clinical Toxicology
URE-K 50%

For external use only. Avoid contact with eyes, lips or mucous membranes. Do not use on areas of broken skin.

Sulfacetamide preparations are incompatible with silver preparations.

After applying this medication, wash hands and unaffected areas thoroughly. Stop use and ask a doctor if redness or irritation develops. If swallowed, get medical help or contact Poison Control Center right away. KEEP THIS AND ALL MEDICATION OUT OF THE REACH OF CHILDREN.

Transient stinging, burning, itching or irritation may occur and normally disappear on discontinuing the medication.

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Tips

Tips

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Interactions

Interactions

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