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  4. NDC Product Code: 82504-104 Legere Lavendar Foot Patch

NDC 82504-104 Legere Lavendar Foot Patch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82504-104?
  4. Legere Lavendar Foot 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:
82504-104
Proprietary Name:
Legere Lavendar Foot Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Myriad Co., Ltd.
Labeler Code:
82504
Product Label ID:
d549f1f3-db14-1534-e053-2a95a90afd29
Start Marketing Date: [9]
01-10-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82504-104-01

Package Description: 40 g in 1 BOX

Product Details

What is NDC 82504-104?

The NDC code 82504-104 is assigned by the FDA to the product Legere Lavendar Foot Patch which is product labeled by Myriad Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82504-104-01 40 g 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 Legere Lavendar Foot Patch?

Adults and children 4 years of age and over: Step 1: Clean and dry area for the patch to be attached.Step 2: Remove the protective cover sheet and gently apply.Step 3: Leave it on at least 4hours before remove.Children under 4years of age: Consult with a doctor.

Which are Legere Lavendar Foot Patch UNII Codes?

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

Which are Legere Lavendar Foot 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".