How Supplied:

How Supplied:
SPL v11
SPL
SPL Set ID b58e175d-60e8-4206-ac7a-c67b68ac80f0
Route
TOPICAL
Published
Effective Date 2025-12-01
Document Type 34391-3 HUMAN PRESCRIPTION DRUG LABEL

Drug Facts

Composition & Product

Identifiers & Packaging


Description

For external use only. Not for ophthalmic use. Keep away from eyes, lips and mucous membranes.


Medication Information

Warnings and Precautions

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

Indications and Usage

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 and ingrown nails.

Dosage and Administration

DOSAGE AND ADMINISTRATION: Apply Urea Nail Gel 45% to diseased or damaged nail tissue twice per day, or as directed by a physician.

Dosage Forms and Strengths

Urea Nail Gel 45% is supplied in a 28 mL glass bottle NDC 42808-0204-28.

Contraindications

CONTRAINDICATIONS: Known hypersensitivity to any of the listed ingredients.

Description

DESCRIPTION: UREA Nail Gel 45% is a keratolytic emollient, which is a gentle, yet potent, tissue softener for nails and/or skin. Each gram of UREA Nail Gel 45% 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:

Section 34080-2

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 Urea Nail Gel 45% is administered to a nursing woman.

Section 34084-4

ADVERSE REACTIONS: Transient stinging, burning, itching or irritation may occur and normally disappear on discontinuing the medication. Call your doctor for medical advice about side effects.

Section 34090-1

CLINICAL PHARMACOLOGY: Urea gently dissolves the intracellular 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.

Section 42228-7

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

Section 42229-5

For external use only. Not for ophthalmic use. Keep away from eyes, lips and mucous membranes.

Section 42232-9

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

Section 43682-4

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

Section 44425-7

Store at controlled room temperature 15 to 30°C (59 to 86°F). Protect from freezing. Manufactured in the U.S.A. for Exact-Rx, Inc., Melville, NY 11747 00-0204-28-205-00 Iss:7/11

Section 51945-4

1

Section 59845-8

DIRECTIONS FOR SKIN: Apply Urea Nail Gel 45% to affected area(s) twice per day, or as directed by a physician. Rub in until gel is absorbed.


Structured Label Content

Indications and Usage (34067-9)

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 and ingrown nails.

Dosage and Administration (34068-7)

DOSAGE AND ADMINISTRATION: Apply Urea Nail Gel 45% to diseased or damaged nail tissue twice per day, or as directed by a physician.

Dosage Forms and Strengths (34069-5)

Urea Nail Gel 45% is supplied in a 28 mL glass bottle NDC 42808-0204-28.

Contraindications (34070-3)

CONTRAINDICATIONS: Known hypersensitivity to any of the listed ingredients.

Warnings and Precautions (34071-1)

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

Section 34080-2 (34080-2)

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 Urea Nail Gel 45% is administered to a nursing woman.

Section 34084-4 (34084-4)

ADVERSE REACTIONS: Transient stinging, burning, itching or irritation may occur and normally disappear on discontinuing the medication. Call your doctor for medical advice about side effects.

Description (34089-3)

DESCRIPTION: UREA Nail Gel 45% is a keratolytic emollient, which is a gentle, yet potent, tissue softener for nails and/or skin. Each gram of UREA Nail Gel 45% 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:

Section 34090-1 (34090-1)

CLINICAL PHARMACOLOGY: Urea gently dissolves the intracellular 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.

Section 42228-7 (42228-7)

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

Section 42229-5 (42229-5)

For external use only. Not for ophthalmic use. Keep away from eyes, lips and mucous membranes.

Section 42232-9 (42232-9)

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

Section 43682-4 (43682-4)

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

Section 44425-7 (44425-7)

Store at controlled room temperature 15 to 30°C (59 to 86°F). Protect from freezing. Manufactured in the U.S.A. for Exact-Rx, Inc., Melville, NY 11747 00-0204-28-205-00 Iss:7/11

Section 51945-4 (51945-4)

1

Section 59845-8 (59845-8)

DIRECTIONS FOR SKIN: Apply Urea Nail Gel 45% to affected area(s) twice per day, or as directed by a physician. Rub in until gel is absorbed.


Raw Label Data

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