Walgreens Pain Relief Gel
NDC Package 0363-5061-33

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

Package Information

Walgreens Pain Relief (benzocaine) gel is do not use tube if it is cut prior to opening cut open tip of tube on score mark use your fingertip or cotton applicator to apply a small pea-size amount of Oral Pain Relief Gel apply to affected area up to four times daily or as directed by a dentist or physician Adults and children 2 years of age and older: Apply to affected area Children under 12 years of age should be supervised in the use of this product Children under 2 years of age: Consult a doctor. This formulation utilizes a gel delivery system. Marketed by Walgreens Company, this product is identified by NDC 0363-5061 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
0363-5061-33
Package Description
1 TUBE in 1 CARTON / 9.35 g in 1 TUBE
Product Code
0363-5061
11-Digit Billing Format
00363506133
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Walgreens Pain Relief
Non-Proprietary Name
Benzocaine
Substance Name
Benzocaine
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
BENZOCAINE 200 mg/g
Pharmacologic Class
Usage Information
Do not use tube if it is cut prior to opening cut open tip of tube on score mark use your fingertip or cotton applicator to apply a small pea-size amount of Oral Pain Relief Gel apply to affected area up to four times daily or as directed by a dentist or physician Adults and children 2 years of age and older: Apply to affected area Children under 12 years of age should be supervised in the use of this product Children under 2 years of age: Consult a doctor

Regulatory & Marketing

Labeler Name
Walgreens Company
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-19-2013
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 0363-5061-33 identifies a specific commercial package of 1 tube in 1 carton / 9.35 g in 1 tube of Walgreens Pain Relief, a human over the counter drug labeled by Walgreens Company. This gel is formulated for oral use and contains benzocaine 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 Walgreens Company on March 19, 2013. The current certification is valid through December 31, 2026.

How is this Walgreens Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00363506133. 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 (4-4-2)
0363-5061-33
11-Digit CMS (5-4-2)
00363-5061-33

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