NDC Package 69842-660-09 3x Medicated Mouth Sore Gel

Benzocaine Gel Oral - 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:
69842-660-09
Package Description:
1 TUBE in 1 CARTON / 11.9 g in 1 TUBE
Product Code:
Proprietary Name:
3x Medicated Mouth Sore Gel
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine; Menthol, Unspecified Form; Zinc Chloride
Usage Information:
Cut open tip of tube on score mark * do not use if tip is cut prior to opening * adults and children 2 years of age and older: apply to affected area up to 4 times daily or as directed by a dentist or doctor. Children under 12 years of age shoul dbe supervised in the use of this product * children under 2 years of age: do not use
11-Digit NDC Billing Format:
69842066009
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:
    Cvs
    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.
  • Sample Package:
    No
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    06-05-2020
    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 69842-660-09?

    The NDC Packaged Code 69842-660-09 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 Cvs. The product's dosage form is gel and is administered via oral form.

    Is NDC 69842-660 included in the NDC Directory?

    Yes, 3x Medicated Mouth Sore Gel with product code 69842-660 is active and included in the NDC Directory. The product was first marketed by Cvs on June 05, 2020 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 69842-660-09?

    The 11-digit format is 69842066009. 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
    5-3-269842-660-095-4-269842-0660-09