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  4. NDC Product Code: 71446-002 Dr Tans Pain Releiving 3 Day Herabl Patch

NDC 71446-002 Dr Tans Pain Releiving 3 Day Herabl Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71446-002?
  4. Dr Tans Pain Releiving 3 Day Herabl Patch 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:
71446-002
Proprietary Name:
Dr Tans Pain Releiving 3 Day Herabl Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Great Loong Llc
Labeler Code:
71446
Product Label ID:
0f1e9bc1-4f15-44a0-bfeb-74002fb0d261
Start Marketing Date: [9]
05-25-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 71446-002?

The NDC code 71446-002 is assigned by the FDA to the product Dr Tans Pain Releiving 3 Day Herabl Patch which is product labeled by Great Loong Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71446-002-01 2 patch in 1 package / .3 g 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 Dr Tans Pain Releiving 3 Day Herabl Patch?

Clean and dry the affected area. Peel film off of patch and apply the herbal-formula side onto the skin. Peel film off the larger dressing patch and apply over the herbal patch to secure it in place. Patch will continue to release herbal formula to the skin for 3 days if desired.

Which are Dr Tans Pain Releiving 3 Day Herabl Patch UNII Codes?

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

Which are Dr Tans Pain Releiving 3 Day Herabl Patch 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".