NDC Package 11822-0316-3 Rite Aid Maximum Strength

Benzocaine Gel, Dentifrice 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:
11822-0316-3
Package Description:
1 TUBE in 1 BLISTER PACK / 9 g in 1 TUBE
Product Code:
Proprietary Name:
Rite Aid Maximum Strength
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
To open tube, cut tip of tube on score mark. adults and children 2 years of age and older: apply to affected area up to 4 times daily or as directed by dentist/doctor. children under 12 years of age: adult supervision should be given in the use of this product.
11-Digit NDC Billing Format:
11822031603
NDC to RxNorm Crosswalk:
  • RxCUI: 238910 - benzocaine 20 % Oral Gel
  • RxCUI: 238910 - benzocaine 0.2 MG/MG Oral Gel
  • RxCUI: 238910 - benzocaine 20 % (180-220 MG per 1 GM) Oral Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Rite Aid
    Dosage Form:
    Gel, Dentifrice - A combination of a dentifrice (formulation intended to clean and/or polish the teeth, and which may contain certain additional agents), and a gel. It is used with a toothbrush for the purpose of cleaning and polishing the teeth.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    M022
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-20-2011
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    11822-0316-41 TUBE in 1 CARTON / 9 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 11822-0316-3?

    The NDC Packaged Code 11822-0316-3 is assigned to a package of 1 tube in 1 blister pack / 9 g in 1 tube of Rite Aid Maximum Strength, a human over the counter drug labeled by Rite Aid. The product's dosage form is gel, dentifrice and is administered via oral form.

    Is NDC 11822-0316 included in the NDC Directory?

    Yes, Rite Aid Maximum Strength with product code 11822-0316 is active and included in the NDC Directory. The product was first marketed by Rite Aid on January 20, 2011 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 11822-0316-3?

    The 11-digit format is 11822031603. 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
    5-4-111822-0316-35-4-211822-0316-03