Medicated
NDC Package 0869-0551-38

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.

Medicated is 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 - do not use, consult a doctorfor best results dry skin thoroughly before applying. Marketed by Vi-jon, this product is identified by NDC 0869-0551 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
0869-0551-38
Package Description
283 g in 1 BOTTLE, DISPENSING
Product Code
0869-0551
11-Digit Billing Format
00869055138
RxNorm Crosswalk
  • RxCUI: 577232 - menthol 0.15 % / zinc oxide 1 % Topical Powder
  • RxCUI: 577232 - menthol 0.0015 MG/MG / zinc oxide 0.01 MG/MG Topical Powder
  • RxCUI: 577232 - Menthol 0.0015 MG/MG / ZNO 0.01 MG/MG Topical Powder

Clinical Specifications

Proprietary Name
Medicated
Dosage Form
-
Usage Information
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 - do not use, consult a doctorfor best results dry skin thoroughly before applying

Regulatory & Marketing

Labeler Name
Vi-jon
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
08-12-2003
Listing Expiration
12-31-2019
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 0869-0551-38 identifies a specific commercial package of 283 g in 1 bottle, dispensing of Medicated, labeled by Vi-jon. 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 Vi-jon on August 12, 2003. The current certification is valid through December 31, 2019.

How is this Vi-jon product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00869055138. 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 (4-4-2)
0869-0551-38
11-Digit CMS (5-4-2)
00869-0551-38

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