Lidopro Patch
NDC Package 83881-403-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Lidopro (lidocaine and menthol) patches is adults and children 12 years of age and over: clean and dry affected area, free of lotions, ointments, and creams. This formulation utilizes a patch delivery system. Marketed by Clinic Pharma, this product is identified by NDC 83881-403 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83881-403-01
Package Description
1 PATCH in 1 POUCH / 10 g in 1 PATCH
Product Code
11-Digit Billing Format
83881040301
RxNorm Crosswalk
  • RxCUI: 1249758 - lidocaine 4 % / menthol 1 % Medicated Patch
  • RxCUI: 1249758 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch
  • RxCUI: 2675625 - LidoPro Pain Relieving Patch 4 % / 1 % Medicated Patch
  • RxCUI: 2675625 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch [LidoPro Pain Relieving Patch]
  • RxCUI: 2675625 - LidoPro Pain Relieving Patch (lidocaine 4 % / menthol 1 % ) Medicated Patch

Clinical Specifications

Proprietary Name
Lidopro
Non-Proprietary Name
Lidocaine And Menthol
Substance Name
Lidocaine; Menthol
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
Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Active Ingredient(s)
Usage Information
Adults and children 12 years of age and over: clean and dry affected area, free of lotions, ointments, and creams. Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Do not use more than one patch in a 12-hour period. Maximum 2 patches per day. Discard patch after single use. Children under 12 years of age: consult a physician.

Regulatory & Marketing

Labeler Name
Clinic Pharma
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-11-2026
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 (83881-403). Click a package code to view its specific billing and regulatory data.

15 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 10 g in 1 PATCH
30 POUCH in 1 CARTON / 1 PATCH in 1 POUCH / 10 g in 1 PATCH

* 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 83881-403-01 identifies a specific commercial package of 1 patch in 1 pouch / 10 g in 1 patch of Lidopro, a human over the counter drug labeled by Clinic Pharma. This patch is formulated for transdermal use and contains lidocaine; 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 Clinic Pharma on March 11, 2026. The current certification is valid through December 31, 2027.

How is this Clinic Pharma product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83881040301. 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)
83881-403-01
11-Digit CMS (5-4-2)
83881-0403-01

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