NDC Package 0280-0039-02 Aleve Arthritis Pain Gel

Diclofenac Sodium 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:
0280-0039-02
Package Description:
1 TUBE in 1 CARTON / 50 g in 1 TUBE
Product Code:
Proprietary Name:
Aleve Arthritis Pain Gel
Non-Proprietary Name:
Diclofenac Sodium
Substance Name:
Diclofenac Sodium
Usage Information:
Diclofenac is used to relieve pain, swelling (inflammation), and joint stiffness caused by arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
11-Digit NDC Billing Format:
00280003902
NDC to RxNorm Crosswalk:
  • RxCUI: 2550740 - Aleve Arthritis Pain 1 % Topical Gel
  • RxCUI: 2550740 - diclofenac sodium 0.01 MG/MG Topical Gel [Aleve Arthritis Pain]
  • RxCUI: 2550740 - Aleve Arthritis Pain 0.01 MG/MG Topical Gel
  • RxCUI: 855633 - diclofenac sodium 1 % Topical Gel
  • RxCUI: 855633 - diclofenac sodium 0.01 MG/MG Topical Gel
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Bayer Healthcare Llc
    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:
    ANDA211253
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    06-01-2021
    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
    0280-0039-011 TUBE in 1 CARTON / 100 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0280-0039-02?

    The NDC Packaged Code 0280-0039-02 is assigned to a package of 1 tube in 1 carton / 50 g in 1 tube of Aleve Arthritis Pain Gel, a human over the counter drug labeled by Bayer Healthcare Llc. The product's dosage form is gel and is administered via topical form.

    Is NDC 0280-0039 included in the NDC Directory?

    Yes, Aleve Arthritis Pain Gel with product code 0280-0039 is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Llc on June 01, 2021 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 0280-0039-02?

    The 11-digit format is 00280003902. 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 4-4-2 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
    4-4-20280-0039-025-4-200280-0039-02