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  5. NDC Package Code: 59088-721-00 Lidocaine Hcl 3% And Hydrocortisone Acetate 0.5% Cream

NDC Package 59088-721-00 Lidocaine Hcl 3% And Hydrocortisone Acetate 0.5% Cream

Lidocaine Hcl And Hydrocortisone Acetate Kit Rectal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
59088-721-00
Package Description:
1 KIT in 1 KIT * 7 g in 1 TUBE (59088-819-01)
Product Code:
59088-721
Proprietary Name:
Lidocaine Hcl 3% And Hydrocortisone Acetate 0.5% Cream
Non-Proprietary Name:
Lidocaine Hcl And Hydrocortisone Acetate
Usage Information:
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.
11-Digit NDC Billing Format:
59088072100
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1012235 - hydrocortisone acetate 0.5 % / lidocaine HCl 3 % Rectal Cream
  • RxCUI: 1012235 - hydrocortisone acetate 5 MG/ML / lidocaine hydrochloride 30 MG/ML Rectal Cream
  • RxCUI: 1012235 - hydrocortisone acetate 0.5 % / lidocaine hydrochloride 3 % Rectal Cream
Product Type:
Human Prescription Drug
Labeler Name:
Puretek Corporation
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s):
Rectal - Administration to the rectum.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
06-30-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 59088-721-00?

The NDC Packaged Code 59088-721-00 is assigned to a package of 1 kit in 1 kit * 7 g in 1 tube (59088-819-01) of Lidocaine Hcl 3% And Hydrocortisone Acetate 0.5% Cream, a human prescription drug labeled by Puretek Corporation. The product's dosage form is kit and is administered via rectal form.

Is NDC 59088-721 included in the NDC Directory?

Yes, Lidocaine Hcl 3% And Hydrocortisone Acetate 0.5% Cream with product code 59088-721 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on June 30, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 59088-721-00?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

What is the 11-digit format for NDC 59088-721-00?

The 11-digit format is 59088072100. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-259088-721-005-4-259088-0721-00