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NDC 82760-005 Arthrimed-plus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82760-005?
  4. Arthrimed-plus 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:
82760-005
Proprietary Name:
Arthrimed-plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Multi Service
Labeler Code:
82760
Product Label ID:
e5316a38-8961-145d-e053-2a95a90ab4a9
Start Marketing Date: [9]
08-02-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82760-005?

The NDC code 82760-005 is assigned by the FDA to the product Arthrimed-plus which is product labeled by Multi Service. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82760-005-01 500 g in 1 bottle, spray . 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 Arthrimed-plus?

For adults and children 2 years of age and older: Shake well before use. Apply to the affected area not more than 3-4 times daily. Allow absorption to occur naturally for maximum penetration. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a health care practitioner.

Which are Arthrimed-plus UNII Codes?

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

Which are Arthrimed-plus 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".