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  4. NDC Product Code: 71183-002 Hot Pain Relief

NDC 71183-002 Hot Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 71183-002?
  5. Hot Pain Relief Uses
  6. Active Ingredients UNII Codes
  7. 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:
71183-002
Proprietary Name:
Hot Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Suzhou Vastech Medical Technology Co., Ltd
Labeler Code:
71183
Product Label ID:
530e42a3-a5d9-1c49-e054-00144ff88e88
Start Marketing Date: [9]
06-28-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Shape:
RECTANGLE (C48347)

Product Packages

NDC Code 71183-002-25

Package Description: 4800 mg in 1 PATCH

Product Details

What is NDC 71183-002?

The NDC code 71183-002 is assigned by the FDA to the product Hot Pain Relief which is product labeled by Suzhou Vastech Medical Technology Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71183-002-25 4800 mg 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 Hot Pain Relief?

DirectionsAdults and Children 12 years of age and over:Clean and dry affected area. Peel off protective film and apply patch once or twice a day. Apply patch an hour after and before shower or bath. Patch will remain effective for 8 hours. Children Under 12 Years of Age: Consult a physician.

Which are Hot Pain Relief UNII Codes?

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

Which are Hot Pain Relief 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".