Mybiooid Lidocaine 4% Pain Relieving Gel-patch
NDC Package 88068-001-01

11-digit billing NDC: 88068000101
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Mybiooid Lidocaine 4% Pain Relieving Gel-patch (lidocaine 4% pain relieving gel-patch) patches is adults and children 12 years of age and over: • clean and dry affected area • remove patch and apply patch to affected area (see illustration) • apply one patch at a time, not more than 3 to 4 times daily • remove patch after no more than 8 hours Children under 12 years: consult a doctor. This formulation utilizes a patch delivery system. Marketed by Avelon Trading Limited, this product is identified by NDC 88068-001 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
88068-001-01
Package Description
15 PATCH in 1 BOX
Product Code
88068-001
11-Digit Billing Format
88068000101

Clinical Specifications

Proprietary Name
Mybiooid Lidocaine 4% Pain Relieving Gel-patch
Non-Proprietary Name
Lidocaine 4% Pain Relieving Gel-patch
Substance Name
Lidocaine
Dosage Form
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
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)
LIDOCAINE 4 g/1001
Pharmacologic Class
Usage Information
Adults and children 12 years of age and over: • clean and dry affected area • remove patch and apply patch to affected area (see illustration) • apply one patch at a time, not more than 3 to 4 times daily • remove patch after no more than 8 hours Children under 12 years: consult a doctor

Regulatory & Marketing

Labeler Name
Avelon Trading Limited
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-14-2026
Listing Expiration
12-31-2027
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (88068-001). Click a package code to view its specific billing and regulatory data.

88068-001-02
33 PATCH in 1 BOX

* 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 88068-001-01 identifies a specific commercial package of 15 patch in 1 box of Mybiooid Lidocaine 4% Pain Relieving Gel-patch, a human over the counter drug labeled by Avelon Trading Limited. This patch is formulated for topical use and contains lidocaine 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 Avelon Trading Limited on October 14, 2026. The current certification is valid through December 31, 2027.

How is this Avelon Trading Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 88068000101. 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)
88068-001-01
11-Digit CMS (5-4-2)
88068-0001-01

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