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  4. NDC Product Code: 43857-0373 Thuja Occidentalis

NDC 43857-0373 Thuja Occidentalis

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0373?
  4. Thuja Occidentalis 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:
43857-0373
Proprietary Name:
Thuja Occidentalis
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bioactive Nutritional, Inc.
Labeler Code:
43857
Product Label ID:
69951bd5-7cd4-4880-b82f-3b453ebd98a3
Start Marketing Date: [9]
07-23-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

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Product Details

What is NDC 43857-0373?

The NDC code 43857-0373 is assigned by the FDA to the product Thuja Occidentalis which is product labeled by Bioactive Nutritional, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43857-0373-1 30 ml in 1 bottle, dispensing . 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 Thuja Occidentalis?

For temporary relief of abdominal pain, rheumatism, and symptoms related to gonorrhea. For temporary relief of abdominal pain, rheumatism, and symptoms related to gonorrhea.

Which are Thuja Occidentalis 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)

Which are Thuja Occidentalis 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".