NDC Package 41250-945-56 Anti-itch

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
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:

41250-945-56

Package Description:

1 TUBE in 1 CARTON / 58 g in 1 TUBE

Product Code:

41250-945

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:

41250094556

Labeler Name:

Meijer, Inc.

Sample Package:

Start Marketing Date:

12-18-2018

Listing Expiration Date:

12-31-2021

Exclude Flag:

Code Structure:

41250 - Meijer, Inc.
- 41250-945 - Anti-itch
  - 41250-945-56 - 1 TUBE in 1 CARTON / 58 g in 1 TUBE

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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
41250-945-28	1 TUBE in 1 CARTON / 28 g in 1 TUBE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 41250-945-56?

The NDC Packaged Code 41250-945-56 is assigned to a package of 1 tube in 1 carton / 58 g in 1 tube of Anti-itch, labeled by Meijer, Inc.. The product's dosage form is and is administered via form.

Is NDC 41250-945 included in the NDC Directory?

No, Anti-itch with product code 41250-945 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Meijer, Inc. on December 18, 2018 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 41250-945-56?

The 11-digit format is 41250094556. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	41250-945-56	5-4-2	41250-0945-56

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