Urea 40% Cream

Urea 40% Cream
SPL v6
SPL
SPL Set ID 6774a5ef-9bb0-4e7a-e053-2a91aa0af47f
Route
TOPICAL
Published
Effective Date 2018-02-01
Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Urea (400 mg)
Inactive Ingredients
Carbomer Interpolymer Type A (55000 Cps) Propylene Glycol Cetyl Alcohol Glyceryl Monostearate Dimethyl Isosorbide Petrolatum Sodium Hydroxide Water Xanthan Gum Mineral Oil

Identifiers & Packaging

Pill Appearance
Color: white
Marketing Status
UNAPPROVED DRUG OTHER Active Since 2018-03-15

Description

Rx Only FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

Dosage and Administration

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

Contraindications

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

Adverse Reactions

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

How Supplied

1 oz. (28.35 g) bottles, NDC 44523-617-01 3 oz. (85 g) bottles, NDC 44523-617-03 7 oz. (198.4 g) bottles, NDC 44523-617-07 To report a serious adverse event or obtain product information, call 1-866-762-2365.


Medication Information

Dosage and Administration

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

Contraindications

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

Adverse Reactions

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

How Supplied

1 oz. (28.35 g) bottles, NDC 44523-617-01 3 oz. (85 g) bottles, NDC 44523-617-03 7 oz. (198.4 g) bottles, NDC 44523-617-07 To report a serious adverse event or obtain product information, call 1-866-762-2365.

Description

Rx Only FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

Section 42229-5

Rx Only



FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

Section 51945-4

Storage:

Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (between 59°F to 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized.

NOTICE:Protect from freezing and excessive heat. Keep bottle tightly closed.

Warning:

KEEP OUT OF REACH OF CHILDREN.

Description:

Each gram contains 400 mg of urea in a vehicle consisting of: carbomer, cetyl alcohol, dimethyl isosorbide, glyceryl stearate, mineral oil, petrolatum, propylene glycol, purified water, sodium hydroxide and xanthan gum.



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

Indications:

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 pilaris, keratosis palmaris, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.

Precautions:

FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.



General:This product 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 and consult a physician.



Information for Patients:Patients should discontinue the use of this product if the condition becomes worse or if a rash develops in the area being treated or elsewhere. Avoid contact with eyes, lips and mucous membranes.

Carcinogenesis, Mutagenesis and Impairment of Fertility:Long-term animal studies for carcinogenic potential have not been performed on this product to date. Studies on reproduction and fertility also have not been performed.



Pregnancy: Category C.Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus.



Nursing Mothers:It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this product is administered to a nursing woman.

How Supplied:

1 oz. (28.35 g) bottles, NDC44523-617-01

3 oz. (85 g) bottles, NDC44523-617-03

7 oz. (198.4 g) bottles, NDC44523-617-07

To reporta serious adverse event or obtain product information, call 1-866-762-2365.

Adverse Reactions:

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

Contraindications:

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

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.



Pharmacokinetics:The mechanism of action of topically applied urea is not yet known.

Dosage and Administration:

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



Apply to diseased or damaged nail(s) twice per day, or as directed by a physician.


Structured Label Content

Section 42229-5 (42229-5)

Rx Only



FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.

Section 51945-4 (51945-4)

Storage: (STORAGE:)

Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C to 30°C (between 59°F to 86°F). Brief exposure to temperatures up to 40°C (104°F) may be tolerated provided the mean kinetic temperature does not exceed 25°C (77°F); however, such exposure should be minimized.

NOTICE:Protect from freezing and excessive heat. Keep bottle tightly closed.

Warning: (WARNING:)

KEEP OUT OF REACH OF CHILDREN.

Description: (DESCRIPTION:)

Each gram contains 400 mg of urea in a vehicle consisting of: carbomer, cetyl alcohol, dimethyl isosorbide, glyceryl stearate, mineral oil, petrolatum, propylene glycol, purified water, sodium hydroxide and xanthan gum.



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

Indications: (INDICATIONS:)

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 pilaris, keratosis palmaris, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.

Precautions: (PRECAUTIONS:)

FOR EXTERNAL USE ONLY. NOT FOR OPHTHALMIC USE.



General:This product 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 and consult a physician.



Information for Patients:Patients should discontinue the use of this product if the condition becomes worse or if a rash develops in the area being treated or elsewhere. Avoid contact with eyes, lips and mucous membranes.

Carcinogenesis, Mutagenesis and Impairment of Fertility:Long-term animal studies for carcinogenic potential have not been performed on this product to date. Studies on reproduction and fertility also have not been performed.



Pregnancy: Category C.Animal reproduction studies have not been conducted with this product. It is also not known whether this product can affect reproduction capacity or cause fetal harm when administered to a pregnant woman. This product should be used by a pregnant woman only if clearly needed or when potential benefits outweigh potential hazards to the fetus.



Nursing Mothers:It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when this product is administered to a nursing woman.

How Supplied: (HOW SUPPLIED:)

1 oz. (28.35 g) bottles, NDC44523-617-01

3 oz. (85 g) bottles, NDC44523-617-03

7 oz. (198.4 g) bottles, NDC44523-617-07

To reporta serious adverse event or obtain product information, call 1-866-762-2365.

Adverse Reactions: (ADVERSE REACTIONS:)

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

Contraindications: (CONTRAINDICATIONS:)

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

Clinical Pharmacology: (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.



Pharmacokinetics:The mechanism of action of topically applied urea is not yet known.

Dosage and Administration: (DOSAGE AND ADMINISTRATION:)

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



Apply to diseased or damaged nail(s) twice per day, or as directed by a physician.


Advanced Ingredient Data


Raw Label Data

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