Urea 40 Percent Cream

Urea 40 Percent Cream
SPL v8
SPL
SPL Set ID d35b75e1-937d-ebc4-e053-2a95a90ac0d8
Route
TOPICAL
Published
Effective Date 2021-11-15
Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Urea (400 mg)
Inactive Ingredients
Glycerin Carbomer Homopolymer, Unspecified Type Cetyl Alcohol White Petrolatum Mineral Oil Water Glyceryl Stearate Se

Identifiers & Packaging

Marketing Status
UNAPPROVED DRUG OTHER Active Since 2021-11-15

Description

INGREDIENTS: Each gram of Urea Cream 40% contains Urea 40% and the following inactive ingredients: Carbomer, Cetearyl Alcohol, Glycerin, Glyceryl Stearate SE, Mineral Oil, Purified Water, White Petrolatum.

Dosage and Administration

Use as directed by your physician. See label booklet for full Prescribing Information.

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

This product is supplied in the following size(s): 3 oz, 1 oz, and 7oz To report a serious adverse event or obtain product information, call 877-250-3427 To report a serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at [email protected]; or call FDA at (800) FDA-1088. Manufactured for: Method Pharmaceuticals, LLC Fort Worth, Texas 76118 Rev. 11/21


Medication Information

Dosage and Administration

Use as directed by your physician. See label booklet for full Prescribing Information.

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

This product is supplied in the following size(s): 3 oz, 1 oz, and 7oz To report a serious adverse event or obtain product information, call 877-250-3427 To report a serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at [email protected]; or call FDA at (800) FDA-1088. Manufactured for: Method Pharmaceuticals, LLC Fort Worth, Texas 76118 Rev. 11/21

Description

INGREDIENTS: Each gram of Urea Cream 40% contains Urea 40% and the following inactive ingredients: Carbomer, Cetearyl Alcohol, Glycerin, Glyceryl Stearate SE, Mineral Oil, Purified Water, White Petrolatum.

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.

Storage:

Store at room

temperature 15°C-30°C

(59°F-86°F).

Protect from freezing.

Keep bottle tightly closed.

Warnings:

FOR   EXTERNAL   USE   ONLY.   NOT   FOR OPHTHALMIC USE. KEEP OUT OF REACH OF CHILDREN.

Avoid contact with eyes, lips and mucous membranes.

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.

Description:

INGREDIENTS: Each gram



of Urea Cream 40%



contains Urea 40% and the



following inactive



ingredients: Carbomer,



Cetearyl Alcohol, Glycerin,



Glyceryl Stearate SE,



Mineral Oil, Purified Water,



White Petrolatum.

Indications:

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.

How Supplied:

This product is supplied in the following size(s): 3 oz, 1 oz, and 7oz

To report a serious adverse event or obtain product information, call 877-250-3427

To report a serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at [email protected]; or call FDA at (800) FDA-1088.

Manufactured for:



Method Pharmaceuticals, LLC Fort Worth, Texas 76118



Rev. 11/21

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.

Pharmacokinetics:

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

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.

Principal Display Panel

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.

Dosage and Administration:

Use as

directed by your physician.

See label booklet for full

Prescribing Information.

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.


Structured Label Content

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.

Storage: (STORAGE:)

Store at room

temperature 15°C-30°C

(59°F-86°F).

Protect from freezing.

Keep bottle tightly closed.

Warnings: (WARNINGS:)

FOR   EXTERNAL   USE   ONLY.   NOT   FOR OPHTHALMIC USE. KEEP OUT OF REACH OF CHILDREN.

Avoid contact with eyes, lips and mucous membranes.

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.

Description: (DESCRIPTION:)

INGREDIENTS: Each gram



of Urea Cream 40%



contains Urea 40% and the



following inactive



ingredients: Carbomer,



Cetearyl Alcohol, Glycerin,



Glyceryl Stearate SE,



Mineral Oil, Purified Water,



White Petrolatum.

Indications: (INDICATIONS:)

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.

How Supplied: (HOW SUPPLIED:)

This product is supplied in the following size(s): 3 oz, 1 oz, and 7oz

To report a serious adverse event or obtain product information, call 877-250-3427

To report a serious adverse event, please contact Method Pharmaceuticals at (877) 250-3427; email at [email protected]; or call FDA at (800) FDA-1088.

Manufactured for:



Method Pharmaceuticals, LLC Fort Worth, Texas 76118



Rev. 11/21

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.

Pharmacokinetics:

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

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.

Principal Display Panel (PRINCIPAL DISPLAY PANEL)

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.

Dosage and Administration: (DOSAGE AND ADMINISTRATION:)

Use as

directed by your physician.

See label booklet for full

Prescribing Information.

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.


Advanced Ingredient Data


Raw Label Data

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