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  4. NDC Product Code: 73729-845 Myosport Relieve Kinesiology

NDC 73729-845 Myosport Relieve Kinesiology

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73729-845?
  4. Myosport Relieve Kinesiology 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:
73729-845
Proprietary Name:
Myosport Relieve Kinesiology
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Patchv3 Vitamins Ltd
Labeler Code:
73729
Product Label ID:
5df9f7fa-2aa5-49c5-96af-d7f7c2ee476a
Start Marketing Date: [9]
06-16-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73729-845-01

Package Description: 1 PATCH in 1 JAR / 2.304 g in 1 PATCH

NDC Code 73729-845-19

Package Description: 19 PATCH in 1 JAR / .12 g in 1 PATCH

Product Details

What is NDC 73729-845?

The NDC code 73729-845 is assigned by the FDA to the product Myosport Relieve Kinesiology which is product labeled by Patchv3 Vitamins Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73729-845-01 1 patch in 1 jar / 2.304 g in 1 patch, 73729-845-19 19 patch in 1 jar / .12 g in 1 patch. 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 Myosport Relieve Kinesiology?

• Adults and children over 12 years• Apply to the affected area not more than 2 to 3 times daily• Each application can be worn not more than 4 days• Store in a cool dry place and in a resalable container

Which are Myosport Relieve Kinesiology UNII Codes?

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

Which are Myosport Relieve Kinesiology 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".