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  5. NDC Package Code: 50730-1512-1 Hemorrhoidal Starch

NDC Package 50730-1512-1 Hemorrhoidal Starch

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:
50730-1512-1
Package Description:
12 SUPPOSITORY in 1 BOX
Product Code:
50730-1512
Proprietary Name:
Hemorrhoidal Starch
Usage Information:
Adults:When practical, cleanse the affected area with mild soap and warm water. Rinse thoroughly.Gently dry by patting or blotting with toilet tissue or soft cloth before application of this product.Detach one suppository from strip of suppositories.Remove film before inserting into the rectum by holding the suppository upright. Carefully separate film by inserting tip of fingernail at film split.Carefully peel film slowly and evenly down both sides to expose suppositoryAvoid excessive handling of suppository, which is designed to melt at body temperature. If suppository seems soft, hold in film wrapper under cold water for 2 or 3 minutes.Insert one suppository rectally up to 6 times daily or after each bowel movementChildren under 12 years: ask a doctor.
11-Digit NDC Billing Format:
50730151201
NDC to RxNorm Crosswalk:
  • RxCUI: 199032 - starch 51 % Rectal Suppository
  • RxCUI: 199032 - starch 0.51 MG/MG Rectal Suppository
    • Labeler Name:
    H And P Industries, Inc. Dba Triad Group
    Sample Package:
    No
    Start Marketing Date:
    08-01-2006
    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 50730-1512-1?

    The NDC Packaged Code 50730-1512-1 is assigned to a package of 12 suppository in 1 box of Hemorrhoidal Starch, labeled by H And P Industries, Inc. Dba Triad Group. The product's dosage form is and is administered via form.

    Is NDC 50730-1512 included in the NDC Directory?

    No, Hemorrhoidal Starch with product code 50730-1512 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by H And P Industries, Inc. Dba Triad Group on August 01, 2006 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 50730-1512-1?

    The 11-digit format is 50730151201. 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 5-4-1 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
    5-4-150730-1512-15-4-250730-1512-01