Rapid Relief Hemorrhoid
NDC Package 82442-030-28

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.

Rapid Relief Hemorrhoid is adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Marketed by Target Corporation, this product is identified by NDC 82442-030 and is authorized under FDA application M015.

Identification & Billing

NDC Package Code
82442-030-28
Package Description
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code
82442-030
11-Digit Billing Format
82442003028
RxNorm Crosswalk
  • RxCUI: 2642220 - glycerin 14.4 % / lidocaine 5 % / phenylephrine HCl 0.25 % / white petrolatum 15 % Rectal Cream
  • RxCUI: 2642220 - glycerin 144 MG/ML / lidocaine 50 MG/ML / petrolatum 150 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Rectal Cream

Clinical Specifications

Proprietary Name
Rapid Relief Hemorrhoid
Dosage Form
-
Usage Information
Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before applying this cream.apply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movementchildren under 12 years of age: ask a doctor

Regulatory & Marketing

Labeler Name
Target Corporation
FDA Application #
M015
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
08-15-2024
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 82442-030-28 identifies a specific commercial package of 1 tube in 1 carton / 28 g in 1 tube of Rapid Relief Hemorrhoid, labeled by Target Corporation. 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 Target Corporation on August 15, 2024. The current certification is valid through December 31, 2025.

How is this Target Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82442003028. 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)
82442-030-28
11-Digit CMS (5-4-2)
82442-0030-28

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