NDC 68007-203 Tianhe Zhuanggu Gao

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68007-203
Proprietary Name:
Tianhe Zhuanggu Gao
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Guilin Tianhe Pharmaceutical Co Ltd
Labeler Code:
68007
Start Marketing Date: [9]
05-25-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68007-203-01

Package Description: 10 PLASTER in 1 BOX

Product Details

What is NDC 68007-203?

The NDC code 68007-203 is assigned by the FDA to the product Tianhe Zhuanggu 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 68007-203-01 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 Zhuanggu Gao?

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

Which are Tianhe Zhuanggu Gao UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Tianhe Zhuanggu 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: 1046551 - camphor 3.22 % / menthol 1.39 % / methyl salicylate 15.01 % Medicated Patch
  • RxCUI: 1046551 - camphor 0.0322 MG/MG / menthol 0.0139 MG/MG / methyl salicylate 0.15 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".