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  4. NDC Product Code: 61045-0002 Arthronew PM

NDC 61045-0002 Arthronew PM

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 61045-0002?
  4. Arthronew PM Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61045-0002
Proprietary Name:
Arthronew PM
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Purecore Wellness, Inc
Labeler Code:
61045
Product Label ID:
3bdf50ce-6909-4db9-8691-a789718466cd
Start Marketing Date: [9]
11-03-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 61045-0002?

The NDC code 61045-0002 is assigned by the FDA to the product Arthronew PM which is product labeled by Purecore Wellness, Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61045-0002-1 57 g in 1 tube . 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 Arthronew PM?

For temporary relief of minor symptoms of joint pain and inflammation. For temporary relief of minor symptoms of joint pain and inflammation.

Which are Arthronew PM UNII Codes?

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

  • ARNICA MONTANA (UNII: O80TY208ZW)
  • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
  • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)

Which are Arthronew PM 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:

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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".