NDC Package 82160-238-01 Cornex

Lactic Acid,Salicylic Acid 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:
82160-238-01
Package Description:
1 TUBE in 1 CARTON / 15 g in 1 TUBE
Product Code:
Proprietary Name:
Cornex
Non-Proprietary Name:
Lactic Acid, Salicylic Acid
Substance Name:
Lactic Acid; Salicylic Acid
Usage Information:
Cornex is used to remove Warts and Corns. A wart is a viral infection of the skin surface layer. The incubation period varies from a few weeks to several months. Warts can be spread by contact of the virus with damaged skin, particularly if warm and moist. This is why one of the most common sources of infection is swimming pools. Corns are hard, thick pads of skin caused by pressure and friction. They usually occur on the feet due to poorly fitting shoes. They can also occur on hands. Cornex Gel is suitable for use by adults, children and the elderly.
11-Digit NDC Billing Format:
82160023801
NDC to RxNorm Crosswalk:
  • RxCUI: 244534 - lactic acid 16.7 % / salicylic acid 16.7 % Topical Gel
  • RxCUI: 244534 - lactic acid 0.167 MG/MG / salicylic acid 0.167 MG/MG Topical Gel
  • RxCUI: 244534 - lactic acid 167 MG / salicylic acid 167 MG per 1 GM Topical Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Pella Pharmaceuticals Co. Ltd
    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.
  • Sample Package:
    No
    FDA Application Number:
    M030
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    03-25-2010
    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 82160-238-01?

    The NDC Packaged Code 82160-238-01 is assigned to a package of 1 tube in 1 carton / 15 g in 1 tube of Cornex, a human over the counter drug labeled by Pella Pharmaceuticals Co. Ltd. The product's dosage form is gel and is administered via topical form.

    Is NDC 82160-238 included in the NDC Directory?

    Yes, Cornex with product code 82160-238 is active and included in the NDC Directory. The product was first marketed by Pella Pharmaceuticals Co. Ltd on March 25, 2010 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 82160-238-01?

    The 11-digit format is 82160023801. 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
    5-3-282160-238-015-4-282160-0238-01