Daylogic Dry Scalp Dandruff
NDC Package 11822-4292-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Daylogic Dry Scalp Dandruff is for maximum dandruff control, use every time you shampoowet hair, massage onto scalp and rinserepeat if desired. Marketed by Rite Aid Corporation, this product is identified by NDC 11822-4292 and is authorized under FDA application part358H.

Identification & Billing

NDC Package Code
11822-4292-2
Package Description
701 mL in 1 BOTTLE, PLASTIC
Product Code
11822-4292
11-Digit Billing Format
11822429202
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Daylogic Dry Scalp Dandruff
Dosage Form
-
Usage Information
For maximum dandruff control, use every time you shampoowet hair, massage onto scalp and rinserepeat if desired

Regulatory & Marketing

Labeler Name
Rite Aid Corporation
FDA Application #
part358H
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-14-2016
Listing Expiration
12-31-2018
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (11822-4292). Click a package code to view its specific billing and regulatory data.

11822-4292-3
701 mL in 1 BOTTLE, PLASTIC

* 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 11822-4292-2 identifies a specific commercial package of 701 ml in 1 bottle, plastic of Daylogic Dry Scalp Dandruff, labeled by Rite Aid Corporation. 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 Rite Aid Corporation on June 14, 2016. The current certification is valid through December 31, 2018.

How is this Rite Aid Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 11822429202. 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 (5-4-1)
11822-4292-2
11-Digit CMS (5-4-2)
11822-4292-02

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