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  4. NDC Product Code: 24909-167 Terrasil Eczema And Psoriasis

NDC 24909-167 Terrasil Eczema And Psoriasis

Thuja Occidentalis,Symphytum Officinale Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 24909-167?
  4. Terrasil Eczema And Psoriasis Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
24909-167
Proprietary Name:
Terrasil Eczema And Psoriasis
Non-Proprietary Name: [1]
Thuja Occidentalis, Symphytum Officinale
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Aidance Skincare & Topical Solutions, Llc
Labeler Code:
24909
Product Label ID:
7b9f390c-f263-46d5-99d5-34dcb865dcbc
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
04-20-2016
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
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Product Details

What is NDC 24909-167?

The NDC code 24909-167 is assigned by the FDA to the product Terrasil Eczema And Psoriasis which is a human over the counter drug product labeled by Aidance Skincare & Topical Solutions, Llc. The generic name of Terrasil Eczema And Psoriasis is thuja occidentalis, symphytum officinale. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 24909-167-99 1 kit in 1 package, combination * 85 g in 1 tube (24909-177-85) * 28 g in 1 tube (24909-187-28). 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 Terrasil Eczema And Psoriasis?

Severe Outbreak Ointment: Massage a small amount into affected skin. Reapply up to 4 times daily. Store at room temperature. May stain fabrics.Daily Care Cream: Massage into affected skin. Reapply up to 4 times daily. Store at room temperature.

Which are Terrasil Eczema And Psoriasis UNII Codes?

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

  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
  • THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
  • SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
  • SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y) (Active Moiety)

Which are Terrasil Eczema And Psoriasis 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

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".