What is NDC 85622-602?

85622-602 is the product NDC for Urevia (urea 39), Urea 390 mg/g cream, listed with the FDA by Blue Heron Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Blue Heron Pharmaceuticals, LLC, NDC labeler code 85622. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Urevia?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Urevia NDC 85622-602 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85622-602Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85622-0602Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
85622-602-04	8562206020485622060204	1 JAR in 1 JAR (85622-602-04) / 113 g in 1 JARMarketed from Jun 4, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Urevia
Generic name (nonproprietary): urea 39
Active ingredients: Urea — 390 mg/g
Dosage form: Cream
Route: Topical
Labeler: Blue Heron Pharmaceuticals, LLCNDC labeler code 85622
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 4, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 85622-602_cf027400-dc2b-4135-88eb-104cfd4c855dSPL ID cf027400-dc2b-4135-88eb-104cfd4c855dSPL set ID 4b130123-4439-42c6-bde1-b3a01cc31eb4RxCUI 1093289UNII 8W8T17847W

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485622060204 followed by a unit qualifier and the quantity

Package 85622-0602-04. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jun 4, 2026.

Indications (excerpt from the label)

Usage: Intensely exfolitating and skin-softening cream with Urea 39%. Helps smooth and soften very, dry, rough, and thickened skin. Suitable for targeted application on areas with very dry, hardened or thick skin, rough patches and calluses, uneven, scaly, or flaky skin texture and thickened nail surface appearance. Helps soften and improve the cosmetic appearance of thickened or irregular nails.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85622-602

What is NDC 85622-602?: 85622-602 is the product NDC for Urevia (urea 39), Urea 390 mg/g cream, listed with the FDA by Blue Heron Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Urevia (Urea 39).
What is the active ingredient?: Urea.
Who is the labeler?: Blue Heron Pharmaceuticals, LLC, NDC labeler code 85622. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Urevia?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Urevia (Urea 39) NDC 85622-602