What is NDC 59088-698?

59088-698 is the product NDC for Urea 39.5% (urea), Urea 395 mg/g cream, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

PureTek Corporation, NDC labeler code 59088. 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 39.5%?

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 39.5% NDC 59088-698 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-698Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0698Add 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
59088-698-16	5908806981659088069816	227 g in 1 JAR (59088-698-16)Marketed from Jan 20, 2023

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 39.5%
Generic name (nonproprietary): urea
Active ingredients: Urea — 395 mg/g
Dosage form: Cream
Route: Topical
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jan 20, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 59088-698_ea2adf3e-cea5-43b2-e053-2995a90a89a6SPL ID ea2adf3e-cea5-43b2-e053-2995a90a89a6SPL set ID ea2adf3e-cea6-43b2-e053-2995a90a89a6RxCUI 2627282UNII 8W8T17847WUPC 0359088698167

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

N459088069816 followed by a unit qualifier and the quantity

Package 59088-0698-16. 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 Jan 20, 2023.

Indications (excerpt from the label)

INDICATIONS & USAGE 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 eshar. 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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-698

What is NDC 59088-698?: 59088-698 is the product NDC for Urea 39.5% (urea), Urea 395 mg/g cream, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Urea 39.5% (Urea).
What is the active ingredient?: Urea.
Who is the labeler?: PureTek Corporation, NDC labeler code 59088. 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 39.5%?: 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 39.5% (Urea) NDC 59088-698