Premieres Pain Spray
NDC Package 32472-102-01

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

Package Information

Premieres Pain (menthol) sprays is for adults and children 2 years of age and older: Shake well and apply to affected area not more than 3-4 times daily. This formulation utilizes a spray delivery system. Marketed by Premiere Enterprises, this product is identified by NDC 32472-102 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
32472-102-01
Package Description
29.5 mL in 1 BOTTLE
Product Code
32472-102
11-Digit Billing Format
32472010201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Premieres Pain
Non-Proprietary Name
Menthol
Substance Name
Menthol
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • 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
For adults and children 2 years of age and older: Shake well and apply to affected area not more than 3-4 times daily. Get extra relief by using after warm shower or bath. Will not stain clothing. For children under 2 years of age, consult a Doctor.

Regulatory & Marketing

Labeler Name
Premiere Enterprises
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-28-2010
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (32472-102). Click a package code to view its specific billing and regulatory data.

32472-102-03
88 mL in 1 BOTTLE
32472-102-04
118 mL in 1 BOTTLE

* 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 32472-102-01 identifies a specific commercial package of 29.5 ml in 1 bottle of Premieres Pain, a human over the counter drug labeled by Premiere Enterprises. This spray is formulated for topical use and contains menthol 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 Premiere Enterprises on December 28, 2010. The current certification is valid through December 31, 2026.

How is this Premiere Enterprises product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 32472010201. 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)
32472-102-01
11-Digit CMS (5-4-2)
32472-0102-01

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