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  4. NDC Product Code: 72584-001 Magictop Pain Relief Patch

NDC 72584-001 Magictop Pain Relief Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72584-001?
  4. Magictop Pain Relief Patch 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:
72584-001
Proprietary Name:
Magictop Pain Relief Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zunyi Jici Bio-health Products Co Ltd
Labeler Code:
72584
Product Label ID:
cf89efcc-9ecf-4415-9bb5-2d538f72ee30
Start Marketing Date: [9]
12-28-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 72584-001?

The NDC code 72584-001 is assigned by the FDA to the product Magictop Pain Relief Patch which is product labeled by Zunyi Jici Bio-health Products Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72584-001-03 3 box in 1 box / 3 patch in 1 box (72584-001-02) / 20 g in 1 patch (72584-001-01). 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 Magictop Pain Relief Patch?

Adults (12 years and older)- Clean and dry the affected area.- Peel film off from patch and apply the herbal formula side onto skin.- Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications.- For the best result, a 2-week course of treatment is recommended.- Children under 12 years: Consult your physician.

Which are Magictop Pain Relief Patch UNII Codes?

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

Which are Magictop Pain Relief Patch 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 Magictop Pain Relief Patch?

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:

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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".