NDC Package 41250-868-10 Hemorrhoidal Pads

Witch Hazel Patch Topical - View Billable Units, 11-Digit Format, RxNorm

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:
41250-868-10
Package Description:
100 PATCH in 1 BOX / 500 mg in 1 PATCH
Product Code:
Proprietary Name:
Hemorrhoidal Pads
Non-Proprietary Name:
Witch Hazel
Substance Name:
Witch Hazel
Usage Information:
As hemorrhoidal treatment for adults:when practical, cleanse the affected area with mild soap and warm water and rinse thoroughly.gently dry by patting or blotting with toilet tissue or soft cloth before applying.gently apply to the affected area by patting and then discard.can be used up to six times daily or after each bowel movement.Children under 12 years of ageconsult a doctor.
11-Digit NDC Billing Format:
41250086810
NDC to RxNorm Crosswalk:
  • RxCUI: 844379 - witch hazel 50 % Medicated Pad
  • RxCUI: 844379 - witch hazel 500 MG/ML Medicated Pad
  • RxCUI: 844379 - witch hazel 50 % Medicated Wipes
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer Distribution Inc.
    Dosage Form:
    Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
    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):
    Sample Package:
    No
    FDA Application Number:
    M015
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-28-2018
    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 41250-868-10?

    The NDC Packaged Code 41250-868-10 is assigned to a package of 100 patch in 1 box / 500 mg in 1 patch of Hemorrhoidal Pads, a human over the counter drug labeled by Meijer Distribution Inc.. The product's dosage form is patch and is administered via topical form.

    Is NDC 41250-868 included in the NDC Directory?

    Yes, Hemorrhoidal Pads with product code 41250-868 is active and included in the NDC Directory. The product was first marketed by Meijer Distribution Inc. on June 28, 2018 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 41250-868-10?

    The 11-digit format is 41250086810. 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
    5-3-241250-868-105-4-241250-0868-10