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  5. NDC Package Code: 54723-999-01 Comfortox Benzocaine

NDC Package 54723-999-01 Comfortox Benzocaine

Benzocaine Cream 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:
54723-999-01
Package Description:
1500 mg in 1 PACKET
Product Code:
54723-999
Proprietary Name:
Comfortox Benzocaine
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
For adults and children two-years or older: Apply to affected area not more then 3 or 4 times daily.  Children under 2 years of age: consult a physician.
11-Digit NDC Billing Format:
54723099901
NDC to RxNorm Crosswalk:
  • RxCUI: 723562 - benzocaine 20 % Topical Cream
  • RxCUI: 723562 - benzocaine 200 MG/ML Topical Cream
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Sambria Pharmaceuticals, Inc.
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    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 20 mg/100mg
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    09-07-2016
    Listing Expiration Date:
    12-31-2024
    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 54723-999-01?

    The NDC Packaged Code 54723-999-01 is assigned to a package of 1500 mg in 1 packet of Comfortox Benzocaine, a human over the counter drug labeled by Sambria Pharmaceuticals, Inc.. The product's dosage form is cream and is administered via topical form.

    Is NDC 54723-999 included in the NDC Directory?

    Yes, Comfortox Benzocaine with product code 54723-999 is active and included in the NDC Directory. The product was first marketed by Sambria Pharmaceuticals, Inc. on September 07, 2016 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 54723-999-01?

    The 11-digit format is 54723099901. 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
    5-3-254723-999-015-4-254723-0999-01