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  5. NDC Package Code: 0363-1605-19 3x Medicated Mouth Sore Gel

NDC Package 0363-1605-19 3x Medicated Mouth Sore Gel

Benzocaine Gel Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
0363-1605-19
Package Description:
1 TUBE in 1 CARTON / 11.9 g in 1 TUBE
Product Code:
0363-1605
Proprietary Name:
3x Medicated Mouth Sore Gel
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine; Menthol, Unspecified Form; Zinc Chloride
Usage Information:
Temporarily relieves pain caused by * canker sores * cold sores * fever blisters * minor irritation or injury of the mouth and gums
11-Digit NDC Billing Format:
00363160519
NDC to RxNorm Crosswalk:
  • RxCUI: 2266762 - benzocaine 20 % / menthol 0.1 % / zinc chloride 0.15 % Oral Gel
  • RxCUI: 2266762 - benzocaine 0.2 MG/MG / menthol 0.001 MG/MG / zinc chloride 0.0015 MG/MG Oral Gel
Product Type:
Human Otc Drug
Labeler Name:
Walgreens
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):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M022
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
10-20-2021
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.

Frequently Asked Questions

What is NDC 0363-1605-19?

The NDC Packaged Code 0363-1605-19 is assigned to a package of 1 tube in 1 carton / 11.9 g in 1 tube of 3x Medicated Mouth Sore Gel, a human over the counter drug labeled by Walgreens. The product's dosage form is gel and is administered via oral form.

Is NDC 0363-1605 included in the NDC Directory?

Yes, 3x Medicated Mouth Sore Gel with product code 0363-1605 is active and included in the NDC Directory. The product was first marketed by Walgreens on October 20, 2021 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 0363-1605-19?

The 11-digit format is 00363160519. 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 4-4-2 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
4-4-20363-1605-195-4-200363-1605-19