NDC 68007-202 Tianhe Gutong Tiegao (in Polyisobutylene Carrier)

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:
68007-202
Proprietary Name:
Tianhe Gutong Tiegao (in Polyisobutylene Carrier)
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]
05-24-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 68007-202-01

Package Description: 4 PATCH in 1 BOX

Product Details

What is NDC 68007-202?

The NDC code 68007-202 is assigned by the FDA to the product Tianhe Gutong Tiegao (in Polyisobutylene Carrier) 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 68007-202-01 4 patch 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 Gutong Tiegao (in Polyisobutylene Carrier)?

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 Gutong Tiegao (in Polyisobutylene Carrier) UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Tianhe Gutong Tiegao (in Polyisobutylene Carrier)?

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: 1046569 - camphor 4 % / capsaicin 0.25 % / menthol 3.05 % Medicated Patch
  • RxCUI: 1046569 - camphor 0.04 MG/MG / capsaicin 0.0025 MG/MG / menthol 0.0305 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".