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NDC 54532-0030 Hevert Detox

Arsenic Trioxide,Clematis Recta Flowering Top,Conium Maculatum Flowering Top,Lachesis Muta - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 54532-0030?
  4. Hevert Detox Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

Get all the details for National Drug Code (NDC) 54532-0030 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
54532-0030
Proprietary Name:
Hevert Detox
Non-Proprietary Name: [1]
Arsenic Trioxide, Clematis Recta Flowering Top, Conium Maculatum Flowering Top, Lachesis Muta Venom, Mercuric Iodide, Phytolacca Americana Root, Toxicodendron Pubescens Shoot, Scrophularia Nodosa Leaf With Stem, Sulfur, Milk Thistle, Chelidonium Majus Root, Taraxacum Officinale, Nitric Acid, Apis Mellifera, Atropa Belladonna, Lytta Vesicatoria, Juniper Berry, Solidago Virgaurea Flowering Top, Eichhornia Crassipes Whole, Okoubaka Aubrevillei Bark, Quassia Amara Wood, And Taraxacum 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]
Hevert Arzneimittel Gmbh & Co Kg
Labeler Code:
54532
Product Label ID:
78e83dc3-182e-4f4f-99df-f39b16953efb
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
09-15-2016
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Code Structure Chart

Product Details

What is NDC 54532-0030?

The NDC code 54532-0030 is assigned by the FDA to the product Hevert Detox which is a human over the counter drug product labeled by Hevert Arzneimittel Gmbh & Co Kg. The generic name of Hevert Detox is arsenic trioxide, clematis recta flowering top, conium maculatum flowering top, lachesis muta venom, mercuric iodide, phytolacca americana root, toxicodendron pubescens shoot, scrophularia nodosa leaf with stem, sulfur, milk thistle, chelidonium majus root, taraxacum officinale, nitric acid, apis mellifera, atropa belladonna, lytta vesicatoria, juniper berry, solidago virgaurea flowering top, eichhornia crassipes whole, okoubaka aubrevillei bark, quassia amara wood, and taraxacum officinale. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 54532-0030-9 1 kit in 1 carton * 50 ml in 1 bottle (54532-0033-5) * 50 ml in 1 bottle (54532-0032-5) * 50 ml in 1 bottle (54532-0031-5) * 50 ml in 1 bottle (54532-0034-5). 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 Hevert Detox?

Hevert Detox Liver:The liquid may be cloudy. Shake well before use.Adults and children over 12 years of age:Take 20 drops in water 3 times daily.Consult a physician for use in children under 12 years of age.Hevert Detox Lymph:Do not use for children under 1 year of age.

Which are Hevert Detox UNII Codes?

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

Which are Hevert Detox 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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".