Uramaxin description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Uramaxin

Medimetriks Pharmaceuticals, Inc.
Groupe PARIMA, Inc.

Uramaxin(45% Urea)GT PRE-FILLED APPLICATOR


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

PATIENT INSTRUCTIONS

1. Apply Uramaxin GT to affected nails or skin twice per day, or as directed by a physician.
2. After application, wipe the tip of the tube to remove excess product. Securely place cap back on the tube.

DESCRIPTION: Uramaxin (45% Urea) GT is a keratolytic emollient, which is a gentle, yet potent, tissue softener for nails and/or skin. Each gram of Uramaxin (45% Urea) GT contains 45% Urea, camphor, edetate disodium, eucalyptus oil, hydroxyethyl cellulose, menthol, propylene glycol and purified water.

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

Uramaxin

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.

PHARMACOKINETICS: The mechanism of action of topically applied Urea is not yet known.

Uses

INDICATIONS AND USES: For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent 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, devitalized and ingrown nails.

CONTRAINDICATIONS: Known hypersensitivity to any of the listed ingredients.

WARNINGS: For external use only. Avoid contact with eyes, lips or mucous membranes.

PRECAUTIONS: This medication is to be used as directed by a physician and should not be used to treat any condition other than that for which it was prescribed. If redness or irritation occurs, discontinue use.

PREGNANCY: Pregnancy Category B. Animal reproduction studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. Because animal reproductive studies are not always predictive of human response, Uramaxin (45% Urea) GT should be given to a pregnant woman only if clearly needed.

NURSING MOTHERS: It is not known whether or not this drug is secreted in human milk. Because many drugs are secreted in human milk, caution should be exercised when Uramaxin (45% Urea) GT is administered to a nursing woman.

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.

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

DOSAGE AND ADMINISTRATION: DIRECTIONS FOR NAILS: Apply Uramaxin (45% Urea) GT to diseased or damaged nail tissue twice per day, or as directed by a physician.

DIRECTIONS FOR SKIN: Apply Uramaxin (45% Urea) GT to affected area(s) twice per day, or as directed by a physician.

HOW SUPPLIED:
Uramaxin (45% Urea) GT 20 mL tube, NDC 43538-250-20

Store at controlled room temperature 15°-30°C (59°-86°F).

Protect from freezing.

Manufactured for:

MEDIMETRIKS
PHARMACEUTICALS, INC.
363 Route 46 West
Fairfield, NJ 07004-2402 USA
www.medimetriks.com

PRINCIPAL DISPLAY PANEL - 20 mL Tube Label

NDC 43538-250-20

Rx Only
Uramaxin ® GT
(45% UREA)
PRE-FILLED APPLICATOR

In a vehicle containing Menthol, Camphor and Eucalyptus Oil

0.68 FL OZ (20 mL)
FOR TOPICAL USE ONLY

MEDIMETRIKS
PHARMACEUTICALS, INC.

Uramaxin

PRINCIPAL DISPLAY PANEL - 20 mL Tube Carton

NDC 43538-250-20

FOR TOPICAL USE ONLY

Rx Only
Uramaxin ® GT
(45% UREA)
PRE-FILLED APPLICATOR

MEDIMETRIKS
PHARMACEUTICALS, INC.

In a vehicle containing Menthol, Camphor and Eucalyptus Oil

0.68 FL OZ (20 mL)

Uramaxin

PRINCIPAL DISPLAY PANEL - 20 mL Tube/255 g Tube Kit Carton

NDC 43538-251-20

Rx Only
Uramaxin ® GT KIT
(45% UREA)

KIT CONTENTS:
1 - 0.68 fl. oz. Uramaxin® (45% Urea) GT Pre-filled Applicator Tube
1 - 9 oz. (255 g) Tube Keradan™ Cream

MEDIMETRIKS
PHARMACEUTICALS, INC.

Uramaxin

Uramaxin

UREA GEL

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:43538-250
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
UREA 0.45 mL

Inactive Ingredients

Ingredient Name Strength
CAMPHOR (SYNTHETIC)
EDETATE DISODIUM
EUCALYPTUS OIL
hydroxyethyl cellulose (4000 mpa.s at 1%)
LEVOMENTHOL
propylene glycol
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 20 in 1 TUBE, WITH APPLICATOR
2 NDC:43538-250-99 5 in 1 TUBE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2010-07-08


Uramaxin GT

Uramaxin GT and Keradan KIT

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:43538-251
Route of Administration DEA Schedule

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:43538-251-20 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
2012-04-15


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.