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  4. NDC Product Code: 46581-685 Salonpas Arthritis Pain

NDC 46581-685 Salonpas Arthritis Pain

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 46581-685?
  4. Salonpas Arthritis Pain Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
46581-685
Proprietary Name:
Salonpas Arthritis Pain
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hisamitsu Pharmaceutical Co., Inc.
Labeler Code:
46581
Product Label ID:
a6518167-fe32-43b2-b736-ba01ac69c12d
Start Marketing Date: [9]
11-01-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 46581-685?

The NDC code 46581-685 is assigned by the FDA to the product Salonpas Arthritis Pain which is product labeled by Hisamitsu Pharmaceutical Co., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 46581-685-09 3 pouch in 1 box / 3 patch in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Salonpas Arthritis Pain?

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

Which are Salonpas Arthritis Pain UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Salonpas Arthritis Pain Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Salonpas Arthritis Pain?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 853146 - menthol 3 % / methyl salicylate 10 % Medicated Patch
  • RxCUI: 853146 - menthol 0.03 MG/MG / methyl salicylate 0.1 MG/MG Medicated Patch

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".