NDC 54256-057 Thuja

  1. Labeler Index
  2. Bioresource Inc.
  3. NDC: 54256-057 Thuja

NDC Product Code 54256-057

NDC CODE: 54256-057

Proprietary Name: Thuja What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: 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.

NDC Code Structure

NDC 54256-057-10

Package Description: 1 BOTTLE, GLASS in 1 BOX > 50 mL in 1 BOTTLE, GLASS

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Thuja with NDC 54256-057 is a product labeled by Bioresource Inc.. The generic name of Thuja is . The product's dosage form is and is administered via form.

Labeler Name: Bioresource Inc.

Dosage Form: -

Product Type: 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.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.
  • ALCOHOL (UNII: 3K9958V90M)

Product Labeler Information

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

Labeler Name: Bioresource Inc.
Labeler Code: 54256
Start Marketing Date: 05-01-2005 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2017 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.
Exclude Flag: I 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Thuja Product Label Images

Thuja Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Otc - Purpose

To minimize adverse acute and chronic vaccination stress reactions.

Dosage

Unless otherwise prescribed, adults take 5 drops orally in liquid, 1 time per day. Children take 3 drops orally in liquid, 1 time per day.

Otc - Ask Doctor

If symptoms persist, contact a licensed practitioner.

Otc - Pregnancy Or Breast Feeding

If you are pregnant or nursing a baby, seek the advice of a health care professional before use.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

Storage And Handling

Protect from light and heat.

Tamper Evident

Do not use this product if tamper evident strip is broken or removed from base of cap.

Ingredients

Thuja occidentalis3X

Inactive Ingredient

Contains 69% alcohol by volume.

Other

Manufactured by:PEKANA® GmbHD-88353 KissleggDistributed by: BioResource Inc.Cotati, CA 94931

* Please review the disclaimer below.