Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis Gel
NDC Package 73287-030-01

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

Package Information

Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis (menthol 8%) gel is for Use By Adults OnlyApply generously to affected area.Massage into painful area until thoroughly absorbed into skin.Repeat as necessary, but no more than 4 times daily. This formulation utilizes a gel delivery system. Marketed by Telebrands Corp, this product is identified by NDC 73287-030 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
73287-030-01
Package Description
1 JAR in 1 CARTON / 85 g in 1 JAR
Product Code
73287-030
11-Digit Billing Format
73287003001

Clinical Specifications

Proprietary Name
Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis
Non-Proprietary Name
Menthol 8%
Substance Name
Menthol
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
MENTHOL 8 g/8g
Usage Information
For Use By Adults OnlyApply generously to affected area.Massage into painful area until thoroughly absorbed into skin.Repeat as necessary, but no more than 4 times daily.

Regulatory & Marketing

Labeler Name
Telebrands Corp
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-02-2024
Listing Expiration
12-31-2026
Exclude Flag
N
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 73287-030-01 identifies a specific commercial package of 1 jar in 1 carton / 85 g in 1 jar of Hempvana Ultra Strength Pain Relief Gel Platinum - Arthritis, a human over the counter drug labeled by Telebrands Corp. This gel is formulated for topical use and contains menthol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Telebrands Corp on September 02, 2024. The current certification is valid through December 31, 2026.

How is this Telebrands Corp product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73287003001. 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)
73287-030-01
11-Digit CMS (5-4-2)
73287-0030-01

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