NDC Package 83881-402-05 Lidopro Patch (lidocaine 4%, Menthol 1%)

Lidocaine And Menthol Patch Patch Transdermal - View Billable Units, 11-Digit Format, RxNorm

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:
83881-402-05
Package Description:
5 mg in 1 POUCH
Product Code:
Proprietary Name:
Lidopro Patch (lidocaine 4%, Menthol 1%)
Non-Proprietary Name:
Lidocaine And Menthol Patch
Substance Name:
Lidocaine; Menthol
Usage Information:
Adults 18 years and older:clean and dry affected areaopen pouch and remove one patchremove protective film from patchapply one patch to the affected area of pain and leave in place for 8 to 12 hours
11-Digit NDC Billing Format:
83881040205
NDC to 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
Product Type:
Human Otc Drug
Labeler Name:
Clinic Pharma
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(s):
Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-09-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N

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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
83881-402-1515 mg in 1 POUCH

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Frequently Asked Questions

What is NDC 83881-402-05?

The NDC Packaged Code 83881-402-05 is assigned to a package of 5 mg in 1 pouch of Lidopro Patch (lidocaine 4%, Menthol 1%), a human over the counter drug labeled by Clinic Pharma. The product's dosage form is patch and is administered via transdermal form.

Is NDC 83881-402 included in the NDC Directory?

Yes, Lidopro Patch (lidocaine 4%, Menthol 1%) with product code 83881-402 is active and included in the NDC Directory. The product was first marketed by Clinic Pharma on January 09, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 83881-402-05?

The 11-digit format is 83881040205. 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
5-3-283881-402-055-4-283881-0402-05