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  5. NDC Package Code: 72667-008-01 Myderm

NDC Package 72667-008-01 Myderm

Lidocaine Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
72667-008-01
Package Description:
237 mL in 1 BOTTLE, PLASTIC
Product Code:
72667-008
Proprietary Name:
Myderm
Non-Proprietary Name:
Lidocaine
Substance Name:
Lidocaine Hydrochloride
Usage Information:
This product is used to help reduce itching and pain from certain skin conditions (such as scrapes, minor skin irritations, insect bites). It may also be used to help relieve nerve pain after shingles (infection with herpes zoster virus). Lidocaine belongs to a class of drugs known as local anesthetics. It works by causing a temporary loss of feeling in the area where you apply the patch.
11-Digit NDC Billing Format:
72667000801
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Inspec Solutions Llc.
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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):
LIDOCAINE HYDROCHLORIDE .5 g/100mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M017
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-26-2019
Listing Expiration Date:
12-31-2026
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
72667-008-02592 mL in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 72667-008-01?

The NDC Packaged Code 72667-008-01 is assigned to a package of 237 ml in 1 bottle, plastic of Myderm, a human over the counter drug labeled by Inspec Solutions Llc.. The product's dosage form is gel and is administered via topical form.

Is NDC 72667-008 included in the NDC Directory?

Yes, Myderm with product code 72667-008 is active and included in the NDC Directory. The product was first marketed by Inspec Solutions Llc. on February 26, 2019 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 72667-008-01?

The 11-digit format is 72667000801. 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
5-3-272667-008-015-4-272667-0008-01