Lidozall Pro Cream
NDC Package 72835-445-05

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Lidozall Pro (lidocaine hydrochloride) cream is for adults and children two-years or older: Apply 1 packet (2 grams) topically to the affected area(s) up to 4 times daily as needed for pain. This formulation utilizes a cream delivery system. Marketed by V2 Pharma Llc, this product is identified by NDC 72835-445 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
72835-445-05
Package Description
5 PACKET in 1 CARTON / 2 g in 1 PACKET
Product Code
72835-445
11-Digit Billing Format
72835044505

Clinical Specifications

Proprietary Name
Lidozall Pro
Non-Proprietary Name
Lidocaine Hydrochloride
Substance Name
Lidocaine Hydrochloride
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
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • 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 4 g/100g
Pharmacologic Class
Usage Information
For adults and children two-years or older: Apply 1 packet (2 grams) topically to the affected area(s) up to 4 times daily as needed for pain. Do not use more than 4 packets (8 grams) per day.

Regulatory & Marketing

Labeler Name
V2 Pharma Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-16-2026
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 72835-445-05 identifies a specific commercial package of 5 packet in 1 carton / 2 g in 1 packet of Lidozall Pro, a human over the counter drug labeled by V2 Pharma Llc. This cream is formulated for topical; topical use and contains lidocaine hydrochloride 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 V2 Pharma Llc on June 16, 2026. The current certification is valid through December 31, 2027.

How is this V2 Pharma Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72835044505. 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)
72835-445-05
11-Digit CMS (5-4-2)
72835-0445-05

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