After Burn Gel
NDC Package 44224-1220-1

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

Package Information

After Burn (2.5% lidocaine hcl) gel is clean rg affected area.Adults and children 2 years of age and older apply a small amount to affected area not more than 3 times daily.Children under 2 years of age consult a doctor. This formulation utilizes a gel delivery system. Marketed by Tender Corporation D/b/a Adventure Ready Brands, this product is identified by NDC 44224-1220 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
44224-1220-1
Package Description
1 TUBE in 1 BOX / 57 g in 1 TUBE (44224-1220-0)
Product Code
44224-1220
11-Digit Billing Format
44224122001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
After Burn
Non-Proprietary Name
2.5% Lidocaine Hcl
Substance Name
Lidocaine Hydrochloride Anhydrous
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
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 ANHYDROUS 1.425 g/57g
Pharmacologic Class
Usage Information
Clean rg affected area.Adults and children 2 years of age and older apply a small amount to affected area not more than 3 times daily.Children under 2 years of age consult a doctor

Regulatory & Marketing

Labeler Name
Tender Corporation D/b/a Adventure Ready Brands
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-11-2024
Listing Expiration
12-31-2026
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 44224-1220-1 identifies a specific commercial package of 1 tube in 1 box / 57 g in 1 tube (44224-1220-0) of After Burn, a human over the counter drug labeled by Tender Corporation D/b/a Adventure Ready Brands. This gel is formulated for topical use and contains lidocaine hydrochloride anhydrous 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 Tender Corporation D/b/a Adventure Ready Brands on November 11, 2024. The current certification is valid through December 31, 2026.

How is this Tender Corporation D/b/a Adventure Ready Brands product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44224122001. 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 (5-4-1)
44224-1220-1
11-Digit CMS (5-4-2)
44224-1220-01

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