Meijer Anti Itch
NDC Package 41250-338-28

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Meijer Anti Itch is direectionsfor itching of skin irritation, inflammation, and rashes:adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: consult a doctorfor external anal and genital itching, adults:when practical, clean the affected area with mild soap and warm water and rinse thoroughlygently dry by patting or blotting with toilet tissue or soft cloth before applyingapply to affected area not more than 3 to 4 times dailychildren under 12 years of age: consult a doctor. Marketed by Meijer, Inc., this product is identified by NDC 41250-338 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
41250-338-28
Package Description
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code
41250-338
11-Digit Billing Format
41250033828
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Meijer Anti Itch
Dosage Form
-
Usage Information
Direectionsfor itching of skin irritation, inflammation, and rashes:adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: consult a doctorfor external anal and genital itching, adults:when practical, clean the affected area with mild soap and warm water and rinse thoroughlygently dry by patting or blotting with toilet tissue or soft cloth before applyingapply to affected area not more than 3 to 4 times dailychildren under 12 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Meijer, Inc.
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
01-15-2015
Listing Expiration
12-31-2021
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 41250-338-28 identifies a specific commercial package of 1 tube in 1 carton / 28 g in 1 tube of Meijer Anti Itch, labeled by Meijer, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Meijer, Inc. on January 15, 2015. The current certification is valid through December 31, 2021.

How is this Meijer, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41250033828. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
41250-338-28
11-Digit CMS (5-4-2)
41250-0338-28

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.