NDC 54256-057 Thuja

Product Information

What is NDC 54256-057?

The NDC code 54256-057 is assigned by the FDA to the product Thuja which is product labeled by Bioresource Inc.. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 54256-057-10 1 bottle, glass in 1 box / 50 ml in 1 bottle, glass. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code54256-057
Proprietary Name 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.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Bioresource Inc.
Labeler Code54256
Start Marketing Date 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 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 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".
NDC Code Structure

What are the uses for Thuja?

Product Packages

NDC Code 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.

Product Details

Thuja Active Ingredients UNII Codes


Thuja 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.

* Please review the disclaimer below.

Thuja Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents

Otc - Purpose

To minimize adverse acute and chronic vaccination stress reactions.


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.


Thuja occidentalis3X

Inactive Ingredient

Contains 69% alcohol by volume.


Manufactured by:
D-88353 Kisslegg

Distributed by: BioResource Inc.
Cotati, CA 94931

Principal Display Panel - 50 Ml Bottle Label


Oral Drops

Homeopathic Medicine

1.7 fl. oz. (50 ml)

* Please review the disclaimer below.