Phoenix Balm
NDC Package 24438-001-02

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

Package Information

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

Phoenix Balm is rub well on the affected area.  Repeat 2 or 3 times daily.For children 2 - 12 years, consult a doctor before use. Marketed by Amazonian Naturals, Inc., this product is identified by NDC 24438-001 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
24438-001-02
Package Description
1 CONTAINER in 1 BOX / 19 g in 1 CONTAINER (24438-001-01)
Product Code
11-Digit Billing Format
24438000102
RxNorm Crosswalk
  • RxCUI: 1232398 - camphor 5 % / menthol 5 % / methyl salicylate 5 % Topical Ointment
  • RxCUI: 1232398 - camphor 0.05 MG/MG / menthol 0.05 MG/MG / methyl salicylate 0.05 MG/MG Topical Ointment

Clinical Specifications

Proprietary Name
Phoenix Balm
Dosage Form
-
Usage Information
Rub well on the affected area.  Repeat 2 or 3 times daily.For children 2 - 12 years, consult a doctor before use.

Regulatory & Marketing

Labeler Name
Amazonian Naturals, Inc.
FDA Application #
part348
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-01-2011
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 24438-001-02 identifies a specific commercial package of 1 container in 1 box / 19 g in 1 container (24438-001-01) of Phoenix Balm, labeled by Amazonian Naturals, 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 Amazonian Naturals, Inc. on December 01, 2011. The current certification is valid through December 31, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24438000102. 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)
24438-001-02
11-Digit CMS (5-4-2)
24438-0001-02

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