Canna Numb Roll On Liquid
NDC Package 72614-265-02

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

Package Information

Canna Numb Roll On (lidocaine hydrochloride, menthol) liquids is adults and children over 12 years:apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour periodmassage into painful area until thoroughly absorbed into skin children 12 years or younger: ask a doctor. This formulation utilizes a liquid delivery system. Marketed by Cannanumb Llc, this product is identified by NDC 72614-265 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
72614-265-02
Package Description
73 mL in 1 CONTAINER
Product Code
72614-265
11-Digit Billing Format
72614026502

Clinical Specifications

Proprietary Name
Canna Numb Roll On
Non-Proprietary Name
Lidocaine Hydrochloride, Menthol
Substance Name
Lidocaine Hydrochloride; 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)
Pharmacologic Class
Usage Information
Adults and children over 12 years:apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour periodmassage into painful area until thoroughly absorbed into skin children 12 years or younger: ask a doctor

Regulatory & Marketing

Labeler Name
Cannanumb Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-01-2018
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 72614-265-02 identifies a specific commercial package of 73 ml in 1 container of Canna Numb Roll On, a human over the counter drug labeled by Cannanumb Llc. This liquid is formulated for topical use and contains lidocaine hydrochloride; 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 Cannanumb Llc on October 01, 2018. The current certification is valid through December 31, 2026.

How is this Cannanumb Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72614026502. 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)
72614-265-02
11-Digit CMS (5-4-2)
72614-0265-02

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