Utaspray Liquid
NDC Package 82198-0008-1

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

Package Information

Utaspray (menthol and methyl salicylate) liquids is clean and dry application area. This formulation utilizes a liquid delivery system. Marketed by Big 5 Nutrition Llc, this product is identified by NDC 82198-0008 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
82198-0008-1
Package Description
70 mL in 1 BOTTLE
Product Code
82198-0008
11-Digit Billing Format
82198000801
RxNorm Crosswalk
  • RxCUI: 1875611 - menthol 10 % / methyl salicylate 5 % Topical Spray
  • RxCUI: 1875611 - menthol 100 MG/ML / methyl salicylate 50 MG/ML Topical Spray

Clinical Specifications

Proprietary Name
Utaspray
Non-Proprietary Name
Menthol And Methyl Salicylate
Substance Name
Menthol; 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)
Usage Information
Clean and dry application area. Spray treatment directly onto skin and gently rub in if desired. May be used up to 10 times per day in adults and children over age 2.

Regulatory & Marketing

Labeler Name
Big 5 Nutrition Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-01-2022
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 82198-0008-1 identifies a specific commercial package of 70 ml in 1 bottle of Utaspray, a human over the counter drug labeled by Big 5 Nutrition Llc. This liquid is formulated for topical use and contains menthol; 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 Big 5 Nutrition Llc on October 01, 2022. The current certification is valid through December 31, 2026.

How is this Big 5 Nutrition Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82198000801. 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 (5-4-1)
82198-0008-1
11-Digit CMS (5-4-2)
82198-0008-01

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