Activon Ultra Strength Arthritis
NDC Package 51068-501-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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.

Activon Ultra Strength Arthritis is 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. Marketed by Family First Pharmaceuticals, Inc., this product is identified by NDC 51068-501 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
51068-501-01
Package Description
1 CANISTER in 1 CARTON / 57 g in 1 CANISTER
Product Code
51068-501
11-Digit Billing Format
51068050101
RxNorm Crosswalk
  • RxCUI: 1148634 - histamine dihydrochloride 0.028 % / menthol 4.57 % Topical Cream
  • RxCUI: 1148634 - histamine dihydrochloride 0.28 MG/ML / menthol 45.7 MG/ML Topical Cream
  • RxCUI: 1148634 - histamine dihydrochloride 0.028 % / menthol 4.574 % Topical Cream
  • RxCUI: 1148636 - ActivOn Ultra Strength Arthritis (histamine dihydrochloride 0.028 % / menthol 4.574 % ) Topical Cream
  • RxCUI: 1148636 - histamine dihydrochloride 0.28 MG/ML / menthol 45.7 MG/ML Topical Cream [ActivOn Arthritis]

Clinical Specifications

Proprietary Name
Activon Ultra Strength Arthritis
Dosage Form
-
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

Regulatory & Marketing

Labeler Name
Family First Pharmaceuticals, Inc.
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
09-01-2011
Listing Expiration
12-31-2017
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51068-501-01 identifies a specific commercial package of 1 canister in 1 carton / 57 g in 1 canister of Activon Ultra Strength Arthritis, labeled by Family First Pharmaceuticals, Inc.. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Family First Pharmaceuticals, Inc. on September 01, 2011. The current certification is valid through December 31, 2017.

How is this Family First Pharmaceuticals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51068050101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
51068-501-01
11-Digit CMS (5-4-2)
51068-0501-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.