1. Home
  2. Labeler Index
  3. Family First Pharmaceuticals, Inc.
  4. 51068-507
  5. NDC Package Code: 51068-507-01 Activon Ultra Strength Arthritis

NDC Package 51068-507-01 Activon Ultra Strength Arthritis

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
51068-507-01
Package Description:
1 CANISTER in 1 CARTON / 57 g in 1 CANISTER
Product Code:
51068-507
Proprietary Name:
Activon Ultra Strength Arthritis
Usage Information:
Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily.children under 12 years of age: ask a doctor
11-Digit NDC Billing Format:
51068050701
NDC to RxNorm Crosswalk:
  • RxCUI: 1148638 - menthol 5.14 % Topical Cream
  • RxCUI: 1148638 - menthol 51.4 MG/ML Topical Cream
  • RxCUI: 1148640 - ActivOn Ultra Strength Joint & Muscle 5.138 % Topical Cream
  • RxCUI: 1148640 - menthol 51.4 MG/ML Topical Cream [ActivOn Joint & Muscle]
  • RxCUI: 1148640 - ActivOn Joint & Muscle 51.4 MG/ML Topical Cream
    • Labeler Name:
    Family First Pharmaceuticals, Inc.
    Sample Package:
    No
    Start Marketing Date:
    02-15-2017
    Listing Expiration Date:
    12-31-2018
    Exclude Flag:
    I
    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 51068-507-01?

    The NDC Packaged Code 51068-507-01 is assigned to a package of 1 canister in 1 carton / 57 g in 1 canister of Activon Ultra Strength Arthritis, labeled by Family First Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.

    Is NDC 51068-507 included in the NDC Directory?

    No, Activon Ultra Strength Arthritis with product code 51068-507 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Family First Pharmaceuticals, Inc. on February 15, 2017 and its listing in the NDC Directory is set to expire on December 31, 2018 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51068-507-01?

    The 11-digit format is 51068050701. 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
    5-3-251068-507-015-4-251068-0507-01