NDC Package 46581-675-09 Salonpas Pain Relief

Menthol,Methyl Salicylate Patch Percutaneous; Topical; Transdermal - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
46581-675-09
Package Description:
3 POUCH in 1 BOX / 3 PATCH in 1 POUCH
Product Code:
Proprietary Name:
Salonpas Pain Relief
Non-Proprietary Name:
Menthol, Methyl Salicylate
Substance Name:
Menthol; Methyl Salicylate
Usage Information:
Adults 18 years and older:only use one patch at a timeclean and dry affected arearemove patch from backing film and apply to skin (see illustration)apply one patch to the affected area and leave in place for up to 8 to 12 hoursif pain lasts after using the first patch, a second patch may be applied for up to another 8 to 12 hoursdo not use more than 2 patches per daydo not use for more than 3 days in a rowthe used patch should be removed from the skin when a new one is appliedChildren under 18 years of age: do not use; this product has not been shown to work in children
11-Digit NDC Billing Format:
46581067509
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
3 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 853146 - menthol 3 % / methyl salicylate 10 % Medicated Patch
  • RxCUI: 853146 - menthol 0.03 MG/MG / methyl salicylate 0.1 MG/MG Medicated Patch
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Hisamitsu Pharmaceutical Co., Inc.
    Dosage Form:
    Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
    Administration Route(s):
  • 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.
  • Sample Package:
    No
    FDA Application Number:
    NDA022029
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    06-01-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    46581-675-011 PATCH in 1 POUCH
    46581-675-991 PATCH in 1 POUCH

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 46581-675-09?

    The NDC Packaged Code 46581-675-09 is assigned to a package of 3 pouch in 1 box / 3 patch in 1 pouch of Salonpas Pain Relief, a human over the counter drug labeled by Hisamitsu Pharmaceutical Co., Inc.. The product's dosage form is patch and is administered via percutaneous; topical; transdermal form.This product is billed for "EA" each discreet unit and contains an estimated amount of 3 billable units per package.

    Is NDC 46581-675 included in the NDC Directory?

    Yes, Salonpas Pain Relief with product code 46581-675 is active and included in the NDC Directory. The product was first marketed by Hisamitsu Pharmaceutical Co., Inc. on June 01, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 46581-675-09?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 3.

    What is the 11-digit format for NDC 46581-675-09?

    The 11-digit format is 46581067509. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-246581-675-095-4-246581-0675-09