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  4. NDC Product Code: 68007-204 Tianhe Zhuifeng Gao

NDC 68007-204 Tianhe Zhuifeng Gao

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68007-204?
  4. Tianhe Zhuifeng Gao Uses
  5. Active Ingredients UNII Codes
  6. 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:
68007-204
Proprietary Name:
Tianhe Zhuifeng Gao
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guilin Tianhe Pharmaceutical Co Ltd
Labeler Code:
68007
Product Label ID:
28457a0b-e7de-4e37-a554-edf4e2000898
Start Marketing Date: [9]
05-27-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 68007-204?

The NDC code 68007-204 is assigned by the FDA to the product Tianhe Zhuifeng Gao which is product labeled by Guilin Tianhe Pharmaceutical Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68007-204-01 10 plaster in 1 box . 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 Tianhe Zhuifeng Gao?

This product is used as PurposeExternal AnalgesicUses  For the temporary relief of minor aches and pains of muscles and jointsdue to:simple backachearthritisstrainsbruisessprains

Which are Tianhe Zhuifeng Gao UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Tianhe Zhuifeng Gao?

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: 1046575 - camphor 4.75 % / capsaicin 0.25 % / menthol 1.4 % Medicated Patch
  • RxCUI: 1046575 - camphor 0.0475 MG/MG / capsaicin 0.0025 MG/MG / menthol 0.014 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".