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Urea 39% Cream

Generic: Urea 39% Cream

Verified·Apr 23, 2026
NDC
44523-801
RxCUI
1093289
Route
TOPICAL
ICD-10 indication
L85.3

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About Urea 39% Cream

What is this medication? Urea 39% Cream is a high-strength topical medication categorized as a keratolytic agent. It is primarily used to treat skin conditions that result in dry, rough, or thickened skin, such as psoriasis, eczema, corns, and calluses. The cream works by softening the keratin in the skin, which helps to dissolve the intercellular matrix and promotes the shedding of dead skin cells. By increasing the skin's ability to hold onto water, it effectively hydrates and smooths areas that have become excessively hardened or scaly. Beyond its use for skin texture, this specific concentration of urea is often prescribed for the treatment of damaged or thickened nails. When applied to a diseased nail plate, the medication softens the nail, making it easier for a healthcare provider to remove or for the patient to gradually debride the area. This process is particularly helpful for managing fungal infections or ingrown nails without the need for invasive surgical procedures. It is important to use this medication exactly as prescribed and to avoid contact with the eyes or sensitive mucous membranes.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Urea 39% Cream. Official source: DailyMed (NLM) · Label effective Jan 13, 2026

Dosage and administration
Apply to affected area(s) twice per day or as directed by a physician. Rub in until completely absorbed.
Contraindications
This product is contraindicated in persons with known or suspected hypersensitivity to any of the ingredients of the product.
Warnings
KEEP OUT OF REACH OF CHILDREN.
Adverse reactions
Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product.
Use in 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.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

Conditions we've indexed resources for

Click a condition to see copay cards, grants, and PA rules specific to it. For the full list of FDA-approved indications, see Prescribing information above.

Prior authorization & coverage

PayerPAStep therapyCopay tier

Medicare Part D

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.