Hemorrhoidal Relief Cream
NDC Package 73622-3077-5

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Hemorrhoidal Relief Cream is adults: when possible, clean affected area with mild soap or warm water, rinse thoroughly, and then gently dry (patting or blotting) with tissue or soft cloth before use to use dispensing cap, attach it to the tube, lubricate well, then gentle insert part way into anus and squeeze tube to deliver medication. Marketed by Curetech Skincare, this product is identified by NDC 73622-3077 and is authorized under FDA application part346.

Identification & Billing

NDC Package Code
73622-3077-5
Package Description
28.3 g in 1 TUBE
Product Code
73622-3077
11-Digit Billing Format
73622307705
RxNorm Crosswalk
  • RxCUI: 2529640 - lidocaine 4 % / phenylephrine hydrochloride 0.25 % Rectal Cream
  • RxCUI: 2529640 - lidocaine 40 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Rectal Cream

Clinical Specifications

Proprietary Name
Hemorrhoidal Relief Cream
Dosage Form
-
Usage Information
Adults: when possible, clean affected area with mild soap or warm water, rinse thoroughly, and then gently dry (patting or blotting) with tissue or soft cloth before use to use dispensing cap, attach it to the tube, lubricate well, then gentle insert part way into anus and squeeze tube to deliver medication. Thoroughly cleanse dispensing cap after use with mild soap and warm water and rinse thoroughlyapply to affected area upto 4 times daily, especially at night, when waking up and after each bowel movementChildren under 12 years of age: ask a doctor

Regulatory & Marketing

Labeler Name
Curetech Skincare
FDA Application #
part346
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
03-04-2021
Listing Expiration
12-31-2022
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 73622-3077-5 identifies a specific commercial package of 28.3 g in 1 tube of Hemorrhoidal Relief Cream, labeled by Curetech Skincare. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Curetech Skincare on March 04, 2021. The current certification is valid through December 31, 2022.

How is this Curetech Skincare product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73622307705. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
73622-3077-5
11-Digit CMS (5-4-2)
73622-3077-05

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.