Leaky Gut Formula Liquid
NDC Package 43742-2091-1
Package Information
Leaky Gut Formula (alfalfa, glycyrrhiza glabra, astacus fluviatilis, berberis aquifolium, lac defloratum, natrum carbonicum, saccharum officinale, aloe, fel tauri, pancreas suis, fragaria vesca, antimonium crudum, carbo vegetabilis, euphorbium officinarum, lycopodium clavatum, magnesia carbonica, zincum metallicum, colibacillinum cum natrum muriaticum, proteus (vulgaris)) liquids is 1-10 drops under the tongue, 3 times a day or as directed by a health professional. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2091.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 12 [hp_X]/mL
- ALOE 7 [hp_X]/mL
- ANTIMONY TRISULFIDE 12 [hp_X]/mL
- ASTACUS ASTACUS 6 [hp_X]/mL
- BERBERIS AQUIFOLIUM ROOT BARK 6 [hp_X]/mL
- BOS TAURUS BILE 8 [hp_X]/mL
- ESCHERICHIA COLI 15 [hp_X]/mL
- EUPHORBIA RESINIFERA RESIN 12 [hp_X]/mL
- FRAGARIA VESCA FRUIT 9 [hp_X]/mL
- GLYCYRRHIZA GLABRA 3 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- MAGNESIUM CARBONATE 12 [hp_X]/mL
- MEDICAGO SATIVA WHOLE 3 [hp_X]/mL
- PROTEUS INCONSTANS 15 [hp_X]/mL
- SKIM MILK 6 [hp_X]/mL
- SODIUM CARBONATE 6 [hp_X]/mL
- SUCROSE 6 [hp_X]/mL
- SUS SCROFA PANCREAS 8 [hp_X]/mL
- ZINC 12 [hp_X]/mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 43742 - Deseret Biologicals, Inc.
- 43742-2091 - Leaky Gut Formula
- 43742-2091-1 - 30 mL in 1 BOTTLE, DROPPER
- 43742-2091 - Leaky Gut Formula
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 43742-2091-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Leaky Gut Formula, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains activated charcoal; aloe; antimony trisulfide; astacus astacus; berberis aquifolium root bark; bos taurus bile; escherichia coli; euphorbia resinifera resin; fragaria vesca fruit; glycyrrhiza glabra; lycopodium clavatum spore; magnesium carbonate; medicago sativa whole; proteus inconstans; skim milk; sodium carbonate; sucrose; sus scrofa pancreas; 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 Deseret Biologicals, Inc. on July 14, 2023. The current certification is valid through December 31, 2026.
How is this Deseret Biologicals, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742209101. 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.