NDC Package 71687-1053-1 Benzodent

Benzocaine Cream Topical - View Billable Units, 11-Digit Format, RxNorm

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:
71687-1053-1
Package Description:
1 TUBE in 1 CARTON / 7 g in 1 TUBE
Product Code:
Proprietary Name:
Benzodent
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
For the temporary relief of pain due to minor irritation of the mouth and gums caused by dentures or orthodontic appliances or injury to mouth and gums.
11-Digit NDC Billing Format:
71687105301
NDC to RxNorm Crosswalk:
  • RxCUI: 1112942 - Benzodent 20 % Topical Cream
  • RxCUI: 1112942 - benzocaine 200 MG/ML Topical Cream [Benzodent]
  • RxCUI: 1112942 - Benzodent 20 % Oromucosal Topical Cream
  • RxCUI: 1112942 - Benzodent 200 MG/ML Topical Cream
  • RxCUI: 723562 - benzocaine 20 % Topical Cream
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Focus Consumer Healthcare, Llc
    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):
    Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    12-08-2017
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    71687-1053-21 TUBE in 1 CARTON / 28 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71687-1053-1?

    The NDC Packaged Code 71687-1053-1 is assigned to a package of 1 tube in 1 carton / 7 g in 1 tube of Benzodent, a human over the counter drug labeled by Focus Consumer Healthcare, Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 71687-1053 included in the NDC Directory?

    Yes, Benzodent with product code 71687-1053 is active and included in the NDC Directory. The product was first marketed by Focus Consumer Healthcare, Llc on December 08, 2017 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 71687-1053-1?

    The 11-digit format is 71687105301. 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
    5-4-171687-1053-15-4-271687-1053-01