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Urea

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Overview

What is Urea 41 Percent?

Each gram contains 410 mg of urea in a vehicle consisting of: ceteareth-25, ceteareth-6, cetyl alcohol, methylparaben, paraffin, propylene glycol, propylparaben, purified water, stearyl alcohol, xanthan gum.

Urea is a diamide of carbonic acid with the following chemical structure:



What does Urea 41 Percent look like?



What are the available doses of Urea 41 Percent?

Sorry No records found.

What should I talk to my health care provider before I take Urea 41 Percent?

Sorry No records found

How should I use Urea 41 Percent?

This product is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, xerosis, ichthyosis, skin cracks and fissures, dermatitis, eczema, psoriasis, keratoses and calluses.

Apply to affected area(s) twice per day or as directed by a physician. Rub in until completely absorbed.

See package insert for full prescribing information.


What interacts with Urea 41 Percent?

Sorry No Records found


What are the warnings of Urea 41 Percent?

Sorry No Records found


What are the precautions of Urea 41 Percent?

Sorry No Records found


What are the side effects of Urea 41 Percent?

Sorry No records found


What should I look out for while using Urea 41 Percent?

This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.

FOR

 

EXTERNAL

 

USE

 

ONLY.

 

NOT

 

FOR

OPHTHALMIC USE. KEEP OUT OF REACH OF CHILDREN.

Avoid contact with eyes, lips and mucous membranes.


What might happen if I take too much Urea 41 Percent?

Sorry No Records found


How should I store and handle Urea 41 Percent?

Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Keep tightly closed (protect from moisture). Protect from light.Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Keep tightly closed (protect from moisture). Protect from light.Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Keep tightly closed (protect from moisture). Protect from light.Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC # 58657-486-08To report a serious adverse event or obtain product information, call 877-250-3427To reporta serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at contact@methodpharm.com; or call FDA at (800) FDA-1088.Manufactured for:Method Pharmaceuticals, LLC Fort Worth, Texas 76118Rev. 04/18This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC # 58657-486-08To report a serious adverse event or obtain product information, call 877-250-3427To reporta serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at contact@methodpharm.com; or call FDA at (800) FDA-1088.Manufactured for:Method Pharmaceuticals, LLC Fort Worth, Texas 76118Rev. 04/18This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC # 58657-486-08To report a serious adverse event or obtain product information, call 877-250-3427To reporta serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at contact@methodpharm.com; or call FDA at (800) FDA-1088.Manufactured for:Method Pharmaceuticals, LLC Fort Worth, Texas 76118Rev. 04/18This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC # 58657-486-08To report a serious adverse event or obtain product information, call 877-250-3427To reporta serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at contact@methodpharm.com; or call FDA at (800) FDA-1088.Manufactured for:Method Pharmaceuticals, LLC Fort Worth, Texas 76118Rev. 04/18


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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 of the skin.

Non-Clinical Toxicology
This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.

FOR

 

EXTERNAL

 

USE

 

ONLY.

 

NOT

 

FOR

OPHTHALMIC USE. KEEP OUT OF REACH OF CHILDREN.

Avoid contact with eyes, lips and mucous membranes.

Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product.

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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

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Interactions

Interactions

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