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UREA
Overview
What is Utopic?
Each gram contains 410 mg of urea in a vehicle consisting of: carbomer, cetyl alcohol, glyceryl stearate, mineral oil, petrolatum, propylene glycol, sodium hydroxide, water and xanthan gum.
Urea is a diamide of carbonic acid with the following chemical structure:
What does Utopic look like?


What are the available doses of Utopic?
Sorry No records found.
What should I talk to my health care provider before I take Utopic?
Sorry No records found
How should I use Utopic?
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.
What interacts with Utopic?
Sorry No Records found
What are the warnings of Utopic?
Sorry No Records found
What are the precautions of Utopic?
Sorry No Records found
What are the side effects of Utopic?
Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product.
What should I look out for while using Utopic?
This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.
KEEP OUT OF REACH OF CHILDREN.
What might happen if I take too much Utopic?
Sorry No Records found
How should I store and handle Utopic?
Store at room temperature between 20C to 25C (68F to 77F), with excursions permitted between 15C to 30C (59F to 86F). Do not store in the refrigerator or freezer. Use nosepiece immediately after removing from foil pouch.This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC 57893-301-08 10 g physician’s sample, NDC 57893-301-10 To reportManufactured for: Artesa Labs, LLC 137585 Research Blvd. Suite 125 Austin, TX 78750 This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC 57893-301-08 10 g physician’s sample, NDC 57893-301-10 To reportManufactured for: Artesa Labs, LLC 137585 Research Blvd. Suite 125 Austin, TX 78750 This product is supplied in the following size(s): 8 oz. (227 g) bottles, NDC 57893-301-08 10 g physician’s sample, NDC 57893-301-10 To reportManufactured for: Artesa Labs, LLC 137585 Research Blvd. Suite 125 Austin, TX 78750
Clinical Information
Chemical Structure
No Image foundClinical 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.
Pharmacokinetics:
Non-Clinical Toxicology
This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.KEEP OUT OF REACH OF CHILDREN.
Systemic clindamycin has been shown to have neuromuscular blocking properties that may enhance the action of other neuromuscular blocking agents. Therefore, it should be used with caution in patients receiving such agents.
FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.
General:
Information for Patients:
Carcinogenesis, Mutagenesis and Impairment of Fertility:
Pregnancy:
Category C.
Nursing Mothers:
Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product.
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.
Review
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. 315.72Tips
Tips
Interactions
Interactions
A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).