Dr Mineral Anti-itch
NDC Package 50499-300-10

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.

Dr Mineral Anti-itch is a medication used as [Uses]Dr. Marketed by Mineralbio, this product is identified by NDC 50499-300 and is authorized under FDA application part349.

Identification & Billing

NDC Package Code
50499-300-10
Package Description
100 mL in 1 BOTTLE, SPRAY
Product Code
50499-300
11-Digit Billing Format
50499030010
RxNorm Crosswalk
  • RxCUI: 1044248 - sodium chloride 0.7 % / menthol 0.05 % Topical Spray
  • RxCUI: 1044248 - menthol 0.5 MG/ML / sodium chloride 0.12 MEQ/ML Topical Spray
  • RxCUI: 1044248 - menthol 0.05 % / sodium chloride 0.7 % Topical Spray
  • RxCUI: 1044248 - Menthol 0.5 MG/ML / NaCl 0.12 MEQ/ML Topical Spray

Clinical Specifications

Proprietary Name
Dr Mineral Anti-itch
Dosage Form
-
Usage Information
This product is used as [Uses]Dr. Mineral Anti-Itch Spray is useful for the temporary relief of itching associated with irritation, rashes and inflammation due to- skin dryness - eczema - psoriasis - photo sensitivity - jewelry - insect bites - soaps and detergents - cosmetics - poison ivy, oak or sumac - seborrheic dermattis - Other use of this product ask a doctor

Regulatory & Marketing

Labeler Name
Mineralbio
FDA Application #
part349
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
02-20-2010
Listing Expiration
12-31-2017
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 50499-300-10 identifies a specific commercial package of 100 ml in 1 bottle, spray of Dr Mineral Anti-itch, labeled by Mineralbio. 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 Mineralbio on February 20, 2010. The current certification is valid through December 31, 2017.

How is this Mineralbio product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50499030010. 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)
50499-300-10
11-Digit CMS (5-4-2)
50499-0300-10

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