K19 Relief Liquid
NDC Package 83574-413-00

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

Package Information

K19 Relief (menthol) liquids is for the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and stains. This formulation utilizes a liquid delivery system. Marketed by K19 Llc, this product is identified by NDC 83574-413 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83574-413-00
Package Description
295 mL in 1 BOTTLE, SPRAY
Product Code
83574-413
11-Digit Billing Format
83574041300
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
K19 Relief
Non-Proprietary Name
Menthol
Substance Name
Menthol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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 12.5 mg/mL
Usage Information
For the temporary relief of minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and stains.

Regulatory & Marketing

Labeler Name
K19 Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-10-2023
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 83574-413-00 identifies a specific commercial package of 295 ml in 1 bottle, spray of K19 Relief, a human over the counter drug labeled by K19 Llc. This liquid 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 K19 Llc on July 10, 2023. The current certification is valid through December 31, 2026.

How is this K19 Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83574041300. 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)
83574-413-00
11-Digit CMS (5-4-2)
83574-0413-00

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