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  5. NDC Package Code: 71680-002-03 Dakota Muscle Relief Roll-on

NDC Package 71680-002-03 Dakota Muscle Relief Roll-on

Menthol,Unspecified Form Solution 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:
71680-002-03
Package Description:
90 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
71680-002
Proprietary Name:
Dakota Muscle Relief Roll-on
Non-Proprietary Name:
Menthol, Unspecified Form
Substance Name:
Menthol, Unspecified Form
Usage Information:
Adults / Children 12 years or older:Shake well before use, test for skin sensitivitySpray directly on affected areaApply externally up to a maximum of 3 to 4 times a dayDo not rub.
11-Digit NDC Billing Format:
71680000203
NDC to RxNorm Crosswalk:
  • RxCUI: 359752 - menthol 6 % Topical Solution
  • RxCUI: 359752 - menthol 60 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Lashe Naturals, Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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, UNSPECIFIED FORM 60 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    part348
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    11-01-2011
    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 71680-002-03?

    The NDC Packaged Code 71680-002-03 is assigned to a package of 90 ml in 1 bottle, with applicator of Dakota Muscle Relief Roll-on, a human over the counter drug labeled by Lashe Naturals, Llc. The product's dosage form is solution and is administered via topical form.

    Is NDC 71680-002 included in the NDC Directory?

    Yes, Dakota Muscle Relief Roll-on with product code 71680-002 is active and included in the NDC Directory. The product was first marketed by Lashe Naturals, Llc on November 01, 2011 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 71680-002-03?

    The 11-digit format is 71680000203. 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
    5-3-271680-002-035-4-271680-0002-03