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  5. NDC Package Code: 41250-797-06 Anti-itch

NDC Package 41250-797-06 Anti-itch

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:
41250-797-06
Package Description:
222 mL in 1 BOTTLE
Product Code:
41250-797
Proprietary Name:
Anti-itch
Usage Information:
This medication is used to temporarily relieve itching and pain caused by minor burns/cuts/scrapes, sunburn, insect bites, minor skin irritations, or rashes from poison ivy, poison oak, or poison sumac. Diphenhydramine belongs to a class of drugs known as antihistamines. It works by blocking the effects of a certain natural substance (histamine) that causes itching. This product may also contain other ingredients (skin protectants such as allantoin, zinc acetate) that may help relieve symptoms such as dry skin, weeping, or oozing. Read the product package for more information. Depending on the brand and the form of diphenhydramine skin product you are using, the package information may state that its use is not recommended in children younger than 2, 6, or 12 years unless directed by the doctor. If you are self-treating with this medication, it is important to read the package instructions carefully before you start using this product to be sure it is right for you. (See also Precautions section.)
11-Digit NDC Billing Format:
41250079706
NDC to RxNorm Crosswalk:
  • RxCUI: 200176 - camphor 0.5 % / menthol 0.5 % Topical Lotion
  • RxCUI: 200176 - camphor 5 MG/ML / menthol 5 MG/ML Topical Lotion
    • Labeler Name:
    Meijer
    Sample Package:
    No
    Start Marketing Date:
    07-02-2012
    Listing Expiration Date:
    12-31-2019
    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 41250-797-06?

    The NDC Packaged Code 41250-797-06 is assigned to a package of 222 ml in 1 bottle of Anti-itch, labeled by Meijer. The product's dosage form is and is administered via form.

    Is NDC 41250-797 included in the NDC Directory?

    No, Anti-itch with product code 41250-797 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Meijer on July 02, 2012 and its listing in the NDC Directory is set to expire on December 31, 2019 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 41250-797-06?

    The 11-digit format is 41250079706. 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
    5-3-241250-797-065-4-241250-0797-06