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  5. NDC Package Code: 61357-135-01 Hemorrodil

NDC Package 61357-135-01 Hemorrodil

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:
61357-135-01
Package Description:
1 BLISTER PACK in 1 CARTON / 12 SUPPOSITORY in 1 BLISTER PACK
Product Code:
61357-135
Proprietary Name:
Hemorrodil
Usage Information:
This product is used as Active IngredientsPurposePhenylephrine Hydrochloride 0.25%VasoconstrictorCocoa Butter 88.44%Protectant. Temporarily shrinks hemorrhoidal tissuesProvides temporary relief from the itching, burning and discomfort associated with hemorrhoidsAids in protecting irritated anorectal areas
11-Digit NDC Billing Format:
61357013501
NDC to RxNorm Crosswalk:
  • RxCUI: 1438497 - cocoa butter 88.4 % / phenylephrine HCl 0.25 % Rectal Suppository
  • RxCUI: 1438497 - cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository
  • RxCUI: 1491717 - Hemorrodil 88.44 % / 0.25 % Rectal Suppository
  • RxCUI: 1491717 - cocoa butter 0.884 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Suppository [Hemorrodil]
  • RxCUI: 1491717 - Hemorrodil (cocoa butter 88.44 % / phenylephrine HCl 0.25 % ) Rectal Suppository
    • Labeler Name:
    Zurich Medical Labs, Llc
    Sample Package:
    No
    Start Marketing Date:
    03-01-1964
    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 61357-135-01?

    The NDC Packaged Code 61357-135-01 is assigned to a package of 1 blister pack in 1 carton / 12 suppository in 1 blister pack of Hemorrodil, labeled by Zurich Medical Labs, Llc. The product's dosage form is and is administered via form.

    Is NDC 61357-135 included in the NDC Directory?

    No, Hemorrodil with product code 61357-135 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Zurich Medical Labs, Llc on March 01, 1964 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 61357-135-01?

    The 11-digit format is 61357013501. 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
    5-3-261357-135-015-4-261357-0135-01