Prequimm Tablet
NDC Package 62630-003-01

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

Package Information

Prequimm (silver nitrate, colchicum autumnale bulb, conium maculatum flowering top, ipecac, strychnos nux vomica seed, pulsatilla pratensis whole, veratrum album root) tablets is adults and children over 12 years:dissolve 2 tablets under the tongue every 15 minutes for 2 hours before chemotherapy,then 2 tablets every 4 hours for 7 to 10 days.Children under 12 years: use half the adult dose. This formulation utilizes a tablet delivery system. Marketed by Zrg Detox, Inc., this product is identified by NDC 62630-003.

Identification & Billing

NDC Package Code
62630-003-01
Package Description
100 TABLET in 1 BOTTLE
Product Code
62630-003
11-Digit Billing Format
62630000301

Clinical Specifications

Proprietary Name
Prequimm
Non-Proprietary Name
Silver Nitrate, Colchicum Autumnale Bulb, Conium Maculatum Flowering Top, Ipecac, Strychnos Nux Vomica Seed, Pulsatilla Pratensis Whole, Veratrum Album Root
Substance Name
Colchicum Autumnale Bulb; Conium Maculatum Flowering Top; Ipecac; Pulsatilla Pratensis Whole; Silver Nitrate; Strychnos Nux-vomica Seed; Veratrum Album Root
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Sublingual - Administration beneath the tongue.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Adults and children over 12 years:dissolve 2 tablets under the tongue every 15 minutes for 2 hours before chemotherapy,then 2 tablets every 4 hours for 7 to 10 days.Children under 12 years: use half the adult dose.

Regulatory & Marketing

Labeler Name
Zrg Detox, 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
10-15-2024
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 62630-003-01 identifies a specific commercial package of 100 tablet in 1 bottle of Prequimm, a human over the counter drug labeled by Zrg Detox, Inc.. This tablet is formulated for sublingual use and contains colchicum autumnale bulb; conium maculatum flowering top; ipecac; pulsatilla pratensis whole; silver nitrate; strychnos nux-vomica seed; veratrum album root 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 Zrg Detox, Inc. on October 15, 2024. The current certification is valid through December 31, 2026.

How is this Zrg Detox, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62630000301. 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 (5-3-2)
62630-003-01
11-Digit CMS (5-4-2)
62630-0003-01

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