Joint-ritis Pain Relieving Roll-on Ointment
NDC Package 83623-161-02

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

Package Information

Joint-ritis Pain Relieving Roll-on (menthol) ointment is • adults and children 12 years of age and older: Apply a small amount gently into affected area not more than three to four times daily • shake well before use • children under 12 years of age: Do not use, consult a doctor. This formulation utilizes a ointment delivery system. Marketed by Lifeline Naturals Of America, Inc., this product is identified by NDC 83623-161 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83623-161-02
Package Description
1 BOTTLE in 1 BOX / 59 mL in 1 BOTTLE (83623-161-22)
Product Code
83623-161
11-Digit Billing Format
83623016102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Joint-ritis Pain Relieving Roll-on
Non-Proprietary Name
Menthol
Substance Name
Menthol, Unspecified Form
Dosage Form
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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, UNSPECIFIED FORM 16 g/100mL
Usage Information
• adults and children 12 years of age and older: Apply a small amount gently into affected area not more than three to four times daily • shake well before use • children under 12 years of age: Do not use, consult a doctor

Regulatory & Marketing

Labeler Name
Lifeline Naturals Of America, Inc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-01-2023
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 83623-161-02 identifies a specific commercial package of 1 bottle in 1 box / 59 ml in 1 bottle (83623-161-22) of Joint-ritis Pain Relieving Roll-on, a human over the counter drug labeled by Lifeline Naturals Of America, Inc.. This ointment is formulated for topical use and contains menthol, unspecified form 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 Lifeline Naturals Of America, Inc. on September 01, 2023. The current certification is valid through December 31, 2026.

How is this Lifeline Naturals Of America, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83623016102. 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)
83623-161-02
11-Digit CMS (5-4-2)
83623-0161-02

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