Universal Arthritis And Sport Liquid
NDC Package 52000-302-33

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Universal Arthritis And Sport (methyl salicylate, capsicum) liquids 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. This formulation utilizes a liquid delivery system. Marketed by Universal Distribution Center Llc, this product is identified by NDC 52000-302 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
52000-302-33
Package Description
473 mL in 1 BOTTLE, PLASTIC
Product Code
52000-302
11-Digit Billing Format
52000030233
RxNorm Crosswalk
  • RxCUI: 2671957 - capsaicin 0.0012 % / methyl salicylate 0.61 % Topical Solution
  • RxCUI: 2671957 - capsaicin 0.012 MG/ML / methyl salicylate 6.1 MG/ML Topical Solution

Clinical Specifications

Proprietary Name
Universal Arthritis And Sport
Non-Proprietary Name
Methyl Salicylate, Capsicum
Substance Name
Capsicum; Methyl Salicylate
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
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)
Pharmacologic Class
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
Universal Distribution Center Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-01-2023
Listing Expiration
12-31-2026
Exclude Flag
N
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 52000-302-33 identifies a specific commercial package of 473 ml in 1 bottle, plastic of Universal Arthritis And Sport, a human over the counter drug labeled by Universal Distribution Center Llc. This liquid is formulated for topical use and contains capsicum; methyl salicylate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Universal Distribution Center Llc on November 01, 2023. The current certification is valid through December 31, 2026.

How is this Universal Distribution Center Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52000030233. 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)
52000-302-33
11-Digit CMS (5-4-2)
52000-0302-33

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