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  5. NDC Package Code: 65923-094-11 Iodent Oral Analgesic

NDC Package 65923-094-11 Iodent Oral Analgesic

Benzocaine Gel Topical - 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:
65923-094-11
Package Description:
1 TUBE in 1 CARTON / 11.9 g in 1 TUBE
Product Code:
65923-094
Proprietary Name:
Iodent Oral Analgesic
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Directionsremove cap and cut tip of tube on score markadults and children 2 years of age and older: apply a small amount of Oral Analgesic Gel to the cavity and around gum surrounding the teeth. Use up to 4 times daily or as directed by a doctor or dentistchildren under 12 years of age: should be supervised in the use of this productchildren under 2 years of age: ask a doctor/dentist
11-Digit NDC Billing Format:
65923009411
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
United Exchange Corp.
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):
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):
BENZOCAINE 200 mg/g
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M022
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-02-2018
Listing Expiration Date:
12-31-2025
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 65923-094-11?

The NDC Packaged Code 65923-094-11 is assigned to a package of 1 tube in 1 carton / 11.9 g in 1 tube of Iodent Oral Analgesic, a human over the counter drug labeled by United Exchange Corp.. The product's dosage form is gel and is administered via topical form.

Is NDC 65923-094 included in the NDC Directory?

Yes, Iodent Oral Analgesic with product code 65923-094 is active and included in the NDC Directory. The product was first marketed by United Exchange Corp. on January 02, 2018 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 65923-094-11?

The 11-digit format is 65923009411. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-265923-094-115-4-265923-0094-11