Hevert Detox Lymph Liquid
NDC Package 54532-0034-5
Package Information
Hevert Detox Lymph (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, and sulfur) liquids is 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.Do not use for children under 1 year of age. This formulation utilizes a liquid delivery system. Marketed by Hevert Arzneimittel Gmbh & Co Kg, this product is identified by NDC 54532-0034.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 6 [hp_X]/50mL
- CLEMATIS RECTA FLOWERING TOP 4 [hp_X]/50mL
- CONIUM MACULATUM FLOWERING TOP 6 [hp_X]/50mL
- LACHESIS MUTA VENOM 8 [hp_X]/50mL
- MERCURIC IODIDE 8 [hp_X]/50mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/50mL
- SCROPHULARIA NODOSA LEAF WITH STEM 3 [hp_X]/50mL
- SULFUR 4 [hp_X]/50mL
- TOXICODENDRON PUBESCENS SHOOT 6 [hp_X]/50mL
Regulatory & Marketing
Hierarchy Structure
- 54532 - Hevert Arzneimittel Gmbh & Co Kg
- 54532-0034 - Hevert Detox Lymph
- 54532-0034-5 - 1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE
- 54532-0034 - Hevert Detox Lymph
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.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 54532-0034-5 identifies a specific commercial package of 1 bottle in 1 carton / 50 ml in 1 bottle of Hevert Detox Lymph, a human over the counter drug labeled by Hevert Arzneimittel Gmbh & Co Kg. This liquid is formulated for oral use and contains arsenic trioxide; clematis recta flowering top; conium maculatum flowering top; lachesis muta venom; mercuric iodide; phytolacca americana root; scrophularia nodosa leaf with stem; sulfur; toxicodendron pubescens shoot 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 June 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: 54532003405. 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.