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  5. NDC Package Code: 55910-402-03 Rexall Maximum Strength Hemorrhoidal

NDC Package 55910-402-03 Rexall Maximum Strength Hemorrhoidal

View Billable Units, 11-Digit Format, RxNorm

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.

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:
55910-402-03
Package Description:
1 TUBE, WITH APPLICATOR in 1 CARTON / 28 g in 1 TUBE, WITH APPLICATOR
Product Code:
55910-402
Proprietary Name:
Rexall Maximum Strength Hemorrhoidal
Usage Information:
Uses- for temporary relief of pain, soreness and burning - helps relieve the local itching and discomfort associated with hemorrhoids - temporarily shrinks hemorrhoidal tissue - temporarily provides a coating for relief of anorectal discomforts - temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful Other information- store at 20 degrees - 25 degrees C (68 degrees - 77 degrees F)- for lot number and expiration date, see crimp of tube or see box
11-Digit NDC Billing Format:
55910040203
NDC to RxNorm Crosswalk:
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine HCl 0.25 % / pramoxine HCl 1 % / white petrolatum 15 % Rectal Cream
  • RxCUI: 1293649 - glycerin 144 MG/ML / petrolatum 150 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 15 % Rectal Cream
    • Labeler Name:
    Dolgencorp, Inc.
    Sample Package:
    No
    Start Marketing Date:
    06-28-2011
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 55910-402-03?

    The NDC Packaged Code 55910-402-03 is assigned to a package of 1 tube, with applicator in 1 carton / 28 g in 1 tube, with applicator of Rexall Maximum Strength Hemorrhoidal, labeled by Dolgencorp, Inc.. The product's dosage form is and is administered via form.

    Is NDC 55910-402 included in the NDC Directory?

    No, Rexall Maximum Strength Hemorrhoidal with product code 55910-402 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Dolgencorp, Inc. on June 28, 2011 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55910-402-03?

    The 11-digit format is 55910040203. 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
    5-3-255910-402-035-4-255910-0402-03