Urea Cream 40%

Urea Cream 40%
SPL v1
SPL
SPL Set ID 0fa4445e-554c-c791-e063-6294a90a9713
Route
TOPICAL
Published
Effective Date 2024-01-23
Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Urea (400 mg)

Identifiers & Packaging

Marketing Status
UNAPPROVED DRUG OTHER Active Since 2024-01-23

Description

This product is a keratolytic emollient which is a gentle, yet potent, tissue softener for nails and/or skin. 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:

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 24470-939-01 3 oz. (85 g) bottles, NDC 24470-939-03 7 oz. (198.4 g) bottles, NDC 24470-939-07 To report a serious adverse event or obtain product information, call 1-855-899-4237. Manufactured for: Cintex Services, LLC 9330 LBJ Freeway, Suite 900 Dallas, TX 75243 2300402 [00] Rev. 12/2023


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 24470-939-01 3 oz. (85 g) bottles, NDC 24470-939-03 7 oz. (198.4 g) bottles, NDC 24470-939-07 To report a serious adverse event or obtain product information, call 1-855-899-4237. Manufactured for: Cintex Services, LLC 9330 LBJ Freeway, Suite 900 Dallas, TX 75243 2300402 [00] Rev. 12/2023

Description

This product is a keratolytic emollient which is a gentle, yet potent, tissue softener for nails and/or skin. 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:

Section 43685-7

WARNINGS: KEEP OUT OF REACH OF CHILDREN.

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.

Section 51945-4

Rx Only

This product is a keratolytic emollient which is a gentle, yet potent, tissue softener for nails and/or skin.

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:

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 container tightly closed.

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.

How Supplied:

1 oz. (28.35 g) bottles, NDC 24470-939-01

3 oz. (85 g) bottles, NDC 24470-939-03

7 oz. (198.4 g) bottles, NDC 24470-939-07

To report a serious adverse event or obtain product information, call 1-855-899-4237.

Manufactured for:

Cintex Services, LLC

9330 LBJ Freeway, Suite 900

Dallas, TX 75243

2300402 [00] Rev. 12/2023

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 43685-7 (43685-7)

WARNINGS: KEEP OUT OF REACH OF CHILDREN.

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.

Section 51945-4 (51945-4)

Rx Only

This product is a keratolytic emollient which is a gentle, yet potent, tissue softener for nails and/or skin.

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:

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 container tightly closed.

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.

How Supplied: (HOW SUPPLIED:)

1 oz. (28.35 g) bottles, NDC 24470-939-01

3 oz. (85 g) bottles, NDC 24470-939-03

7 oz. (198.4 g) bottles, NDC 24470-939-07

To report a serious adverse event or obtain product information, call 1-855-899-4237.

Manufactured for:

Cintex Services, LLC

9330 LBJ Freeway, Suite 900

Dallas, TX 75243

2300402 [00] Rev. 12/2023

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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