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  5. NDC Package Code: 83574-413-00 K19 Relief

NDC Package 83574-413-00 K19 Relief

Menthol Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
83574-413-00
Package Description:
295 mL in 1 BOTTLE, SPRAY
Product Code:
83574-413
Proprietary Name:
K19 Relief
Non-Proprietary Name:
Menthol
Substance Name:
Menthol
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.
11-Digit NDC Billing Format:
83574041300
NDC to RxNorm Crosswalk:
  • RxCUI: 1606487 - menthol 1.25 % Topical Spray
  • RxCUI: 1606487 - menthol 12.5 MG/ML Topical Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    K19 Llc
    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(s):
  • 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
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-10-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 83574-413-00?

    The NDC Packaged Code 83574-413-00 is assigned to a package of 295 ml in 1 bottle, spray of K19 Relief, a human over the counter drug labeled by K19 Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 83574-413 included in the NDC Directory?

    Yes, K19 Relief with product code 83574-413 is active and included in the NDC Directory. The product was first marketed by K19 Llc on July 10, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 83574-413-00?

    The 11-digit format is 83574041300. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-283574-413-005-4-283574-0413-00