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  4. NDC Product Code: 66506-181 Cheezheng Pain Relieving

NDC 66506-181 Cheezheng Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66506-181?
  4. Cheezheng Pain Relieving 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:
66506-181
Proprietary Name:
Cheezheng Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tibet Cheezheng Tibetan Medicine Co. Ltd.
Labeler Code:
66506
Product Label ID:
ec226931-ef3b-4592-bc95-f5e90cb46690
Start Marketing Date: [9]
01-20-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 66506-181-01

Package Description: 8 h in 1 PATCH

Product Details

What is NDC 66506-181?

The NDC code 66506-181 is assigned by the FDA to the product Cheezheng Pain Relieving which is product labeled by Tibet Cheezheng Tibetan Medicine Co. Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66506-181-01 8 h 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 Cheezheng Pain Relieving?

For adults and children 12 years of age and over, apply to the affected areas as described in the diagram to the right.Use one or two plasters daily as needed.Do not apply to extremely hairy skin. Highly adhesive plaster may hurt skin upon removal.Apply the plaster on the affected area and keep it on for 4-8 hours.

Which are Cheezheng Pain Relieving UNII Codes?

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

Which are Cheezheng Pain Relieving 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".