NDC Package 70372-723-02 Lidoplus Pain Relief

Lidocaine Hydrochloride Cream Topical - View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

70372-723-02

Package Description:

5 mL in 1 PACKET

Product Code:

70372-723

Proprietary Name:

Lidoplus Pain Relief

Non-Proprietary Name:

Lidocaine Hydrochloride

Substance Name:

Lidocaine Hydrochloride

Usage Information:

For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites and minor skin irritations.

11-Digit NDC Billing Format:

70372072302

NDC to RxNorm Crosswalk:

RxCUI: 1010895 - lidocaine HCl 4 % Topical Cream

RxCUI: 1010895 - lidocaine hydrochloride 40 MG/ML Topical Cream

RxCUI: 1010895 - lidocaine hydrochloride 4 % Topical Cream

Product Type:

Human Otc Drug

Labeler Name:

Centura Pharmaceuticals, Inc

Dosage Form:

Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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 40 mg/mL

Pharmacologic Class(es):

Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)

Amides - [CS]

Antiarrhythmic - [EPC] (Established Pharmacologic Class)

Local Anesthesia - [PE] (Physiologic Effect)

Sample Package:

FDA Application Number:

M017

Marketing Category:

OTC MONOGRAPH DRUG -

Start Marketing Date:

12-25-2015

Listing Expiration Date:

12-31-2025

Exclude Flag:

Code Structure:

70372 - Centura Pharmaceuticals, Inc
- 70372-723 - Lidoplus Pain Relief
  - 70372-723-02 - 5 mL in 1 PACKET

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 Code	Package Description
70372-723-01	1 TUBE in 1 BOX / 118 mL in 1 TUBE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70372-723-02?

The NDC Packaged Code 70372-723-02 is assigned to a package of 5 ml in 1 packet of Lidoplus Pain Relief, a human over the counter drug labeled by Centura Pharmaceuticals, Inc. The product's dosage form is cream and is administered via topical form.

Is NDC 70372-723 included in the NDC Directory?

Yes, Lidoplus Pain Relief with product code 70372-723 is active and included in the NDC Directory. The product was first marketed by Centura Pharmaceuticals, Inc on December 25, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70372-723-02?

The 11-digit format is 70372072302. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	70372-723-02	5-4-2	70372-0723-02

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