What is NDC 59088-731?

59088-731 is the product NDC for Xyliderm kit, 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?

Xyliderm (Lidocaine, Isopropyl Alcohol).

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 Xyliderm?

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.

Xyliderm NDC 59088-731 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-731Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0731Add 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
59088-731-00	5908807310059088073100	1 KIT in 1 KIT (59088-731-00) * 30 POUCH in 1 PACKAGE (59088-905-54) / 1 PATCH in 1 POUCH (59088-905-84) * 200 PACKET in 1 BOX (53329-805-60) / 1 APPLICATOR in 1 PACKET / 5 mL in 1 APPLICATORMarketed from Jul 5, 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): Xyliderm
Generic name (nonproprietary): lidocaine, isopropyl alcohol
Dosage form: Kit
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jul 5, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 59088-731_292ffe3d-5894-5477-e063-6294a90a708aSPL ID 292ffe3d-5894-5477-e063-6294a90a708aSPL set ID fed45e06-cc4d-fbc5-e053-6294a90a1b19RxCUI 797544, 1745091, 2642344

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N459088073100 followed by a unit qualifier and the quantity

Package 59088-0731-00. 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 Dec 13, 2024.

Indications (excerpt from the label)

INDICATION AND USAGE Lidocan™ is indicated for relief of pain associated with post-herpetic neuralgia. It should be applied only to intact skin.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-731

What is NDC 59088-731?: 59088-731 is the product NDC for Xyliderm kit, 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?: Xyliderm (Lidocaine, Isopropyl Alcohol).
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 Xyliderm?: 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.

Xyliderm (Lidocaine, isopropyl alcohol) NDC 59088-731