What is NDC 87021-602?

87021-602 is the product NDC for Urea 39 (urea), Urea 390 mg/g cream, listed with the FDA by Krewe Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Krewe Pharma, LLC, NDC labeler code 87021. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Urea 39?

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.

Urea 39 NDC 87021-602 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)87021-602Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87021-0602Add 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
87021-602-04	8702106020487021060204	1 JAR in 1 JAR (87021-602-04) / 113 g in 1 JARMarketed from Jun 2, 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): Urea 39
Generic name (nonproprietary): urea
Active ingredients: Urea — 390 mg/g
Dosage form: Cream
Route: Topical
Labeler: Krewe Pharma, LLCNDC labeler code 87021
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 2, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 87021-602_c298ff83-acc1-4dcd-8eb9-2b2d3a57439cSPL ID c298ff83-acc1-4dcd-8eb9-2b2d3a57439cSPL set ID be19358f-67a8-4a0d-88e0-91eb4cb42e0dRxCUI 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

N487021060204 followed by a unit qualifier and the quantity

Package 87021-0602-04. 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 2, 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 87021-602

What is NDC 87021-602?: 87021-602 is the product NDC for Urea 39 (urea), Urea 390 mg/g cream, listed with the FDA by Krewe Pharma, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Urea 39 (Urea).
What is the active ingredient?: Urea.
Who is the labeler?: Krewe Pharma, LLC, NDC labeler code 87021. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Urea 39?: 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.

Urea 39 (Urea) NDC 87021-602