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  4. NDC Product Code: 24909-158 Terrasil Serious First Aid

NDC 24909-158 Terrasil Serious First Aid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 24909-158?
  4. Terrasil Serious First Aid Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory .
NDC Product Code:
24909-158
Proprietary Name:
Terrasil Serious First Aid
Product Type: [3]
Labeler Name: [5]
Aidance Skincare & Topical Solutions, Llc
Labeler Code:
24909
Product Label ID:
3c232eeb-1e11-418c-97be-7bb3b819e3aa
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
01-01-2018
End Marketing Date: [10]
06-01-2020
Listing Expiration Date: [11]
06-01-2020
Exclude Flag: [12]
D
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Product Details

What is NDC 24909-158?

The NDC code 24909-158 is assigned by the FDA to the product Terrasil Serious First Aid which is product labeled by Aidance Skincare & Topical Solutions, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24909-158-28 28 g in 1 tube . 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 Serious First Aid?

Wash and dry affected skin. Apply an ample amount of ointment. Cover with a clean bandage. Repeat procedure 1 to 3 times daily until skin improves or as directed by a doctor. Store at room temperature. May stain fabrics.

Which are Terrasil Serious First Aid UNII Codes?

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

  • THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N)
  • THUJA OCCIDENTALIS WHOLE (UNII: 5HBV6WCE3N) (Active Moiety)

Which are Terrasil Serious First Aid 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.

[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.

[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

[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".