NDC Package 82617-105-60 The Solution Numbing

Lidocaine Hydrochloride Gel 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:
82617-105-60
Package Description:
60 mL in 1 BOTTLE
Product Code:
Proprietary Name:
The Solution Numbing
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
ADULTCLEANSE THE AFFECTED AREA WITH: MILD SOAP AND WARM WATER AND RINSE THOROUGHLY/BY PATTING OR BLOTTING WITH AN APPROPRIATE CLEANSING PAD.GENTLY DRY BY PATTING OR BLOTTING WITH TOILET TISSUE OR A SOFT CLOTH BEFORE APPLICATION OF THIS PRODUCTCHILDREN UNDER 12 YEARS OF AGE: CONSULT A PHYSICIANAPPLY EXTERNALLY TO THE AFFECTED AREA UP TO 6 TIMES DAILYDO NOT USE MORE OFTEN THAN DIRECTEDGENTLY APPLY TO THE AFFECTED AREA BY PATTING AND THEN DISCARD (PAD)
11-Digit NDC Billing Format:
82617010560
NDC to RxNorm Crosswalk:
  • RxCUI: 1245194 - lidocaine HCl 5 % Rectal Gel
  • RxCUI: 1245194 - lidocaine hydrochloride 0.05 MG/MG Rectal Gel
  • RxCUI: 1245194 - lidocaine hydrochloride 5 % Rectal Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Scalp Tech Inc
    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):
  • 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:
    05-12-2024
    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 82617-105-60?

    The NDC Packaged Code 82617-105-60 is assigned to a package of 60 ml in 1 bottle of The Solution Numbing, a human over the counter drug labeled by Scalp Tech Inc. The product's dosage form is gel and is administered via topical form.

    Is NDC 82617-105 included in the NDC Directory?

    Yes, The Solution Numbing with product code 82617-105 is active and included in the NDC Directory. The product was first marketed by Scalp Tech Inc on May 12, 2024 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 82617-105-60?

    The 11-digit format is 82617010560. 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
    5-3-282617-105-605-4-282617-0105-60