Detox Liquid
NDC Package 70558-0004-1

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

Package Information

Detox (beta vulgaris, boldo, chelidonium majus, sarsaparilla (smilax regelii), gelsemium sempervirens, veratrum album, ferrum metallicum, iodium, lycopodium clavatum, nux vomica, pulsatilla (vulgaris), selenium metallicum, thuja occidentalis, zincum metallicum) liquids is for temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Pro Weight Loss Inc., this product is identified by NDC 70558-0004.

Identification & Billing

NDC Package Code
70558-0004-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
70558-0004
11-Digit Billing Format
70558000401

Clinical Specifications

Proprietary Name
Detox
Non-Proprietary Name
Beta Vulgaris, Boldo, Chelidonium Majus, Sarsaparilla (smilax Regelii), Gelsemium Sempervirens, Veratrum Album, Ferrum Metallicum, Iodium, Lycopodium Clavatum, Nux Vomica, Pulsatilla (vulgaris), Selenium Metallicum, Thuja Occidentalis, Zincum Metallicum
Substance Name
Beta Vulgaris; Chelidonium Majus; Gelsemium Sempervirens Root; Iodine; Iron; Lycopodium Clavatum Spore; Peumus Boldus Leaf; Pulsatilla Vulgaris Whole; Selenium; Smilax Ornata Root; Strychnos Nux-vomica Seed; Thuja Occidentalis Leafy Twig; Veratrum Album Root; Zinc
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)
Pharmacologic Class
Usage Information
For temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to excretory dysfunction including mucous congestion.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Pro Weight Loss Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
10-18-2018
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 70558-0004-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Detox, a human over the counter drug labeled by Pro Weight Loss Inc.. This liquid is formulated for oral use and contains beta vulgaris; chelidonium majus; gelsemium sempervirens root; iodine; iron; lycopodium clavatum spore; peumus boldus leaf; pulsatilla vulgaris whole; selenium; smilax ornata root; strychnos nux-vomica seed; thuja occidentalis leafy twig; veratrum album root; zinc 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 Pro Weight Loss Inc. on October 18, 2018. The current certification is valid through December 31, 2026.

How is this Pro Weight Loss Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70558000401. 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)
70558-0004-1
11-Digit CMS (5-4-2)
70558-0004-01

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