Salonpas Pain Relieving Jet Aerosol, Spray
NDC Package 46581-440-99

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

Salonpas Pain Relieving Jet (menthol, methyl salicylate) aerosols is adults and children 12 years of age and over:shake the can very well before use to avoid frostbite, hold the can 4 inches (10 cm) away from the skin, and spray each affected area for no longer than 1 secondapply to affected area not more than 3 to 4 times dailyChildren under 12 years of age: consult a docutor. This formulation utilizes a aerosol, spray delivery system. Marketed by Hisamitsu Pharmaceutical Co., Inc., this product is identified by NDC 46581-440 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
46581-440-99
Package Description
3.6 g in 1 CAN
Product Code
46581-440
11-Digit Billing Format
46581044099
RxNorm Crosswalk
  • RxCUI: 1101083 - menthol 3 % / methyl salicylate 10 % Topical Spray
  • RxCUI: 1101083 - menthol 30 MG/ML / methyl salicylate 100 MG/ML Topical Spray

Clinical Specifications

Proprietary Name
Salonpas Pain Relieving Jet
Non-Proprietary Name
Menthol, Methyl Salicylate
Substance Name
Menthol; Methyl Salicylate
Dosage Form
Aerosol, Spray - An aerosol product which utilizes a compressed gas as the propellant to provide the force necessary to expel the product as a wet spray; it is applicable to solutions of medicinal agents in aqueous solvents.
Administration Route
  • Percutaneous - Administration through the skin.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Transdermal - Administration through the dermal layer of the skin to the systemic circulation by diffusion.
Active Ingredient(s)
Usage Information
Adults and children 12 years of age and over:shake the can very well before use to avoid frostbite, hold the can 4 inches (10 cm) away from the skin, and spray each affected area for no longer than 1 secondapply to affected area not more than 3 to 4 times dailyChildren under 12 years of age: consult a docutor

Regulatory & Marketing

Labeler Name
Hisamitsu Pharmaceutical Co., Inc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-01-2011
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 (46581-440). Click a package code to view its specific billing and regulatory data.

46581-440-04
14.6 g in 1 CAN

* 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 46581-440-99 identifies a specific commercial package of 3.6 g in 1 can of Salonpas Pain Relieving Jet, a human over the counter drug labeled by Hisamitsu Pharmaceutical Co., Inc.. This aerosol, spray is formulated for percutaneous; topical; transdermal 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 Hisamitsu Pharmaceutical Co., Inc. on May 01, 2011. The current certification is valid through December 31, 2026.

How is this Hisamitsu Pharmaceutical Co., Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 46581044099. 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)
46581-440-99
11-Digit CMS (5-4-2)
46581-0440-99

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