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  5. NDC Package Code: 69626-0049-4 Tanac Oral Pain Reliever

NDC Package 69626-0049-4 Tanac Oral Pain Reliever

Benzocaine Liquid 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:
69626-0049-4
Package Description:
1 BOTTLE in 1 CARTON / 13.3 mL in 1 BOTTLE
Product Code:
69626-0049
Proprietary Name:
Tanac Oral Pain Reliever
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Apply product with cotton swab or clean fingertip to the affected areaadults and children 2 years of age and older: use up times 4 times daily or as directed by a dentist or doctor. Children should be supervised in the use of this product.children under 2 years of age: do not use
11-Digit NDC Billing Format:
69626004904
NDC to RxNorm Crosswalk:
  • RxCUI: 1053339 - Tanac Liquid 10 % Mucous Membrane Topical Solution
  • RxCUI: 1053339 - benzocaine 100 MG/ML Mucous Membrane Topical Solution [Tanac Liquid]
  • RxCUI: 1053339 - Tanac Liquid 100 MG/ML Mucous Membrane Topical Solution
  • RxCUI: 583152 - benzocaine 10 % Mucous Membrane Topical Solution
  • RxCUI: 583152 - benzocaine 100 MG/ML Mucous Membrane Topical Solution
Product Type:
Human Otc Drug
Labeler Name:
Leosons Overseas Corp
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
BENZOCAINE 10 g/100mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M022
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
01-01-2015
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 69626-0049-4?

The NDC Packaged Code 69626-0049-4 is assigned to a package of 1 bottle in 1 carton / 13.3 ml in 1 bottle of Tanac Oral Pain Reliever, a human over the counter drug labeled by Leosons Overseas Corp. The product's dosage form is liquid and is administered via oral form.

Is NDC 69626-0049 included in the NDC Directory?

Yes, Tanac Oral Pain Reliever with product code 69626-0049 is active and included in the NDC Directory. The product was first marketed by Leosons Overseas Corp on January 01, 2015 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 69626-0049-4?

The 11-digit format is 69626004904. 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 5-4-1 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
5-4-169626-0049-45-4-269626-0049-04