Hevert Detox Intestinum Liquid
NDC Package 54532-0031-5

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Hevert Detox Intestinum (eichhornia crassipes whole, okoubaka aubrevillei bark, quassia amara wood, and taraxacum officinale) 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. This formulation utilizes a liquid delivery system. Marketed by Hevert Arzneimittel Gmbh & Co Kg, this product is identified by NDC 54532-0031.

Identification & Billing

NDC Package Code
54532-0031-5
Package Description
1 BOTTLE in 1 CARTON / 50 mL in 1 BOTTLE
Product Code
54532-0031
11-Digit Billing Format
54532003105

Clinical Specifications

Proprietary Name
Hevert Detox Intestinum
Non-Proprietary Name
Eichhornia Crassipes Whole, Okoubaka Aubrevillei Bark, Quassia Amara Wood, And Taraxacum Officinale
Substance Name
Eichhornia Crassipes Whole; Okoubaka Aubrevillei Bark; Quassia Amara Wood; Taraxacum Officinale
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
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.

Regulatory & Marketing

Labeler Name
Hevert Arzneimittel Gmbh & Co Kg
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-15-2016
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 54532-0031-5 identifies a specific commercial package of 1 bottle in 1 carton / 50 ml in 1 bottle of Hevert Detox Intestinum, a human over the counter drug labeled by Hevert Arzneimittel Gmbh & Co Kg. This liquid is formulated for oral use and contains eichhornia crassipes whole; okoubaka aubrevillei bark; quassia amara wood; taraxacum officinale 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: 54532003105. 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:

10-Digit Format (5-4-1)
54532-0031-5
11-Digit CMS (5-4-2)
54532-0031-05

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.