Hevert Detox Kit
NDC Package 54532-0030-9
Package Information
Hevert Detox (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) kits is hevert Detox Liver:The liquid may be cloudy. This formulation utilizes a kit delivery system. Marketed by Hevert Arzneimittel Gmbh & Co Kg, this product is identified by NDC 54532-0030.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 54532 - Hevert Arzneimittel Gmbh & Co Kg
- 54532-0030 - Hevert Detox
- 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)
- 54532-0030 - Hevert Detox
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 54532-0030-9 identifies a specific commercial package of 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) of Hevert Detox, a human over the counter drug labeled by Hevert Arzneimittel Gmbh & Co Kg. This kit is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Hevert Arzneimittel Gmbh & Co Kg on September 15, 2016. The current certification is valid through December 31, 2026.
How is this Hevert Arzneimittel Gmbh & Co Kg product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 54532003009. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.