Hemorrhoid Anesthetic
NDC Package 52000-028-37

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.

Hemorrhoid Anesthetic is usesFor the temporary relief of local anorectal burning and discomfort associated with hemmorrhoids, anorectal disorders, inflamed hemorrhoidal tissues or piles. Marketed by Universal Distribution Center Llc, this product is identified by NDC 52000-028 and is authorized under FDA application M015.

Identification & Billing

NDC Package Code
52000-028-37
Package Description
1 TUBE in 1 CARTON / 28 g in 1 TUBE (52000-028-39)
Product Code
52000-028
11-Digit Billing Format
52000002837
RxNorm Crosswalk
  • RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine HCl 0.25 % Rectal Ointment
  • RxCUI: 1372298 - mineral oil 0.14 MG/MG / petrolatum 0.749 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Ointment
  • RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine hydrochloride 0.25 % Rectal Ointment

Clinical Specifications

Proprietary Name
Hemorrhoid Anesthetic
Dosage Form
-
Usage Information
UsesFor the temporary relief of local anorectal burning and discomfort associated with hemmorrhoids, anorectal disorders, inflamed hemorrhoidal tissues or piles.

Regulatory & Marketing

Labeler Name
Universal Distribution Center Llc
FDA Application #
M015
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-05-2016
Listing Expiration
12-31-2025
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 52000-028-37 identifies a specific commercial package of 1 tube in 1 carton / 28 g in 1 tube (52000-028-39) of Hemorrhoid Anesthetic, labeled by Universal Distribution Center Llc. 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 Universal Distribution Center Llc on August 05, 2016. The current certification is valid through December 31, 2025.

How is this Universal Distribution Center Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52000002837. 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 (5-3-2)
52000-028-37
11-Digit CMS (5-4-2)
52000-0028-37

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