What is NDC 59088-721?

59088-721 is the product NDC for Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream 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?

Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream (Lidocaine HCl and Hydrocortisone Acetate).

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 Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream?

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.

NDC 59088-721

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-721Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0721Add 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
59088-721-00	5908807210059088072100	1 KIT in 1 KIT (59088-721-00) * 7 g in 1 TUBE (59088-819-01)Marketed from Jun 30, 2025

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): Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream
Generic name (nonproprietary): lidocaine hcl and hydrocortisone acetate
Dosage form: Kit
Route: Rectal
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 30, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 59088-721_399b5b61-0a1b-80f2-e063-6394a90a6163SPL ID 399b5b61-0a1b-80f2-e063-6394a90a6163SPL set ID 3881327f-c3fc-7df2-e063-6294a90a468dRxCUI 1012235UPC 0359088721001

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

N459088072100 followed by a unit qualifier and the quantity

Package 59088-0721-00. 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 Jul 10, 2025.

Indications (excerpt from the label)

INDICATIONS: Indicated for the anti-inflammatory and anesthetic relief of itching, pain, soreness and discomfort due to hemorrhoids, anal fissures, pruritus ani and similar conditions of the anal area.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59088-721

What is NDC 59088-721?: 59088-721 is the product NDC for Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream 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?: Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream (Lidocaine HCl and Hydrocortisone Acetate).
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 Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream?: 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.

Lidocaine HCl 3% and Hydrocortisone Acetate 0.5% Cream (Lidocaine hcl and hydrocortisone acetate) NDC 59088-721