Gluten Detox Liquid
NDC Package 50845-0234-2

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

Package Information

Gluten Detox (barley (grain), carbo vegetabilis, cinchona officinalis, gluten, glyphosate, hydrastis canadensis, lycopodium clavatum, natrum muriaticum, nux vomica, oat (grain), pancreas suis, pulsatilla (vulgaris), rye (grain), wheat (grain)) liquids May temporarily relieve symptoms related to reactions to gluten, such as:• bloating• brain fog• poor digestion• abdominal pain• alternating constipation and diarrhea****These statements are based upon traditional homeopathic practice. This formulation utilizes a liquid delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0234.

Identification & Billing

NDC Package Code
50845-0234-2
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0234-1)
Product Code
50845-0234
11-Digit Billing Format
50845023402

Clinical Specifications

Proprietary Name
Gluten Detox
Non-Proprietary Name
Barley (grain), Carbo Vegetabilis, Cinchona Officinalis, Gluten, Glyphosate, Hydrastis Canadensis, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Oat (grain), Pancreas Suis, Pulsatilla (vulgaris), Rye (grain), Wheat (grain)
Substance Name
Activated Charcoal; Barley; Cinchona Officinalis Bark; Glyphosate; Goldenseal; Lycopodium Clavatum Spore; Oatmeal; Pulsatilla Vulgaris Whole; Rye; Sodium Chloride; Strychnos Nux-vomica Seed; Sus Scrofa Pancreas; Wheat; Wheat Gluten
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
May temporarily relieve symptoms related to reactions to gluten, such as:• bloating• brain fog• poor digestion• abdominal pain• alternating constipation and diarrhea****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. May temporarily relieve symptoms related to reactions to gluten, such as:• bloating• brain fog• poor digestion• abdominal pain• alternating constipation and diarrhea****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Liddell Laboratories, 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
05-23-2017
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 50845-0234-2 identifies a specific commercial package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0234-1) of Gluten Detox, a human over the counter drug labeled by Liddell Laboratories, Inc.. This liquid is formulated for oral use and contains activated charcoal; barley; cinchona officinalis bark; glyphosate; goldenseal; lycopodium clavatum spore; oatmeal; pulsatilla vulgaris whole; rye; sodium chloride; strychnos nux-vomica seed; sus scrofa pancreas; wheat; wheat gluten 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 Liddell Laboratories, Inc. on May 23, 2017. The current certification is valid through December 31, 2026.

How is this Liddell Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845023402. 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)
50845-0234-2
11-Digit CMS (5-4-2)
50845-0234-02

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