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Uredex

urea · Uredex is a prescription drug containing urea, made by Blue Heron Pharmaceuticals, LLC.

Type
Prescription
Drug class
Not classified
Route
Topical
Manufacturers
1

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.

Related recalls

FDA drug recalls that name this drug or its active ingredient

All drug recalls

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

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.

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 mucousmembranes. 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.

Side effects (adverse reactions)

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

Description

Each gram contains 200 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: Figure 1

How supplied

3 oz. (85 g) bottles, NDC 85622-0601-03 To report a serious adverse event or obtain product information, call (813) 380-0271. Manufactured for: Blue Heron Pharmacueticals, LLC 2831 Allegra Way, Suite 218, Lutz, FL 33559 Questions? Call: (813) 380-0271

Storage and handling

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.

Forms and strengths

From the FDA NDC Directory · 1 product codes

Dosage formStrengthRouteNDCs
Cream200 mg/gtopical1

Side effect reports to FDA

FDA Adverse Event Reporting System (FAERS), 2,154 reports that list urea, data through 07/30/2026

Anyone can report a problem to FDA, and a report does not mean the drug caused the problem. Reports can be duplicated or incomplete, and counts depend on how widely a drug is used. Do not stop or change a medicine because of this list. Talk to your doctor or pharmacist.

Most often reported reactions

  • Diarrhea189
  • Fatigue180
  • Nausea157
  • Off label use151
  • Drug ineffective115
  • Decreased appetite108
  • Rash105
  • Vomiting102
  • Dyspnea101
  • Pain98

To report a side effect, use FDA MedWatch.

Manufacturers and labels

1 FDA label

  • Blue Heron Pharmaceuticals, LLCShown hereLabel 07/13/2026 · NDC 85622-601Full label

Uredex: common questions

What is Uredex used for?
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.
What are the side effects of Uredex?
Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product. See the full side effects section on this page, and ask your doctor or pharmacist about any side effect that bothers you.
Is Uredex a prescription drug?
Yes. Uredex is a prescription (Rx) drug.
Are there other products with the same active ingredient as Uredex?
Yes. Other FDA-listed products with the same active ingredients include Urea, Urea 41%, Urea Cream 40%, Urea 40 Percent.

Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 07/13/2026 · Label text is shown as published by the manufacturer. Not medical advice

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