Kaseha Pain Relieving Gel
NDC Package 83056-002-02
Package Information
Kaseha Pain Relieving Gel is a . Marketed by Denali Natural Products, this product is identified by NDC 83056-002 and is authorized under FDA application M017.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 83056 - Denali Natural Products
- 83056-002 - Kaseha Pain Relieving Gel
- 83056-002-02 - 60 mL in 1 JAR
- 83056-002 - Kaseha Pain Relieving Gel
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 83056-002-02 identifies a specific commercial package of 60 ml in 1 jar of Kaseha Pain Relieving Gel, labeled by Denali Natural Products. 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 Denali Natural Products on April 07, 2023. The current certification is valid through April 07, 2023.
How is this Denali Natural Products product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 83056000202. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.