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  5. NDC Package Code: 10202-526-20 7 Select Hemorrhoidal Original Strength

NDC Package 10202-526-20 7 Select Hemorrhoidal Original Strength

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:
10202-526-20
Package Description:
1 TUBE, WITH APPLICATOR in 1 BOX / 20 g in 1 TUBE, WITH APPLICATOR
Product Code:
10202-526
Proprietary Name:
7 Select Hemorrhoidal Original Strength
Usage Information:
Directionsadults: 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 ointment.when first opening the tube, remove foil sealapply to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movement
11-Digit NDC Billing Format:
10202052620
NDC to RxNorm Crosswalk:
  • RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine HCl 0.25 % Rectal Ointment
  • RxCUI: 1372298 - mineral oil 0.14 MG/MG / petrolatum 0.749 MG/MG / phenylephrine hydrochloride 0.0025 MG/MG Rectal Ointment
  • RxCUI: 1372298 - mineral oil 14 % / petrolatum 74.9 % / phenylephrine hydrochloride 0.25 % Rectal Ointment
    • Labeler Name:
    7-eleven, Inc.
    Sample Package:
    No
    Start Marketing Date:
    12-07-2016
    Listing Expiration Date:
    12-31-2021
    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 10202-526-20?

    The NDC Packaged Code 10202-526-20 is assigned to a package of 1 tube, with applicator in 1 box / 20 g in 1 tube, with applicator of 7 Select Hemorrhoidal Original Strength, labeled by 7-eleven, Inc.. The product's dosage form is and is administered via form.

    Is NDC 10202-526 included in the NDC Directory?

    No, 7 Select Hemorrhoidal Original Strength with product code 10202-526 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by 7-eleven, Inc. on December 07, 2016 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 10202-526-20?

    The 11-digit format is 10202052620. 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
    5-3-210202-526-205-4-210202-0526-20