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  5. NDC Package Code: 82442-030-28 Rapid Relief Hemorrhoid

NDC Package 82442-030-28 Rapid Relief Hemorrhoid

14.4% Glycerin,0.25% Phenylephrine Hcl,5% Lidocaine,15% Petrolatum Cream Topical - 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:
82442-030-28
Package Description:
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code:
82442-030
Proprietary Name:
Rapid Relief Hemorrhoid
Non-Proprietary Name:
14.4% Glycerin, 0.25% Phenylephrine Hcl, 5% Lidocaine, 15% Petrolatum
Substance Name:
Glycerin; Lidocaine; Petrolatum; Phenylephrine Hydrochloride
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
11-Digit NDC Billing Format:
82442003028
NDC to 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
Product Type:
Human Otc Drug
Labeler Name:
Target Corporation
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M015
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-15-2024
Listing Expiration Date:
12-31-2025
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 82442-030-28?

The NDC Packaged Code 82442-030-28 is assigned to a package of 1 tube in 1 carton / 28 g in 1 tube of Rapid Relief Hemorrhoid, a human over the counter drug labeled by Target Corporation. The product's dosage form is cream and is administered via topical form.

Is NDC 82442-030 included in the NDC Directory?

Yes, Rapid Relief Hemorrhoid with product code 82442-030 is active and included in the NDC Directory. The product was first marketed by Target Corporation on August 15, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 82442-030-28?

The 11-digit format is 82442003028. 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
5-3-282442-030-285-4-282442-0030-28