Leaky Gut Formula

Product NDC
43742-1903
Requested package NDC
43742-1903-1
11-digit product format
437421903
Labeler code
43742
Product ID
43742-1903_9fcb2b7a-778d-4826-ac32-5e7827b70bc1
Type
HUMAN OTC DRUG
Nonproprietary name
Alfalfa, Glycyrrhiza Glabra, Aloe, Astacus Fluviatilis, Berberis Aquifolium, Lac Defloratum, Natrum Carbonicum, Saccharum Officinale, Fel Tauri, Pancreas Suis, Pancreatinum, Fragaria Vesca, Antimonium Crudum, Carbo Vegetabilis, Euphorbium Officinarum, Lycopodium Clavatum, Magnesia Carbonica, Zincum Metallicum, Colibacillinum Cum Natrum Muriaticum, Proteus (Vulgaris)
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-10-23
Marketing end
2025-12-02
Substance
MEDICAGO SATIVA WHOLE; GLYCYRRHIZA GLABRA; ALOE; ASTACUS ASTACUS; BERBERIS AQUIFOLIUM ROOT BARK; SKIM MILK; SODIUM CARBONATE; SUCROSE; BOS TAURUS BILE; SUS SCROFA PANCREAS; PANCRELIPASE; FRAGARIA VESCA FRUIT; ANTIMONY TRISULFIDE; ACTIVATED CHARCOAL; EUPHORBIA RESINIFERA RESIN; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CARBONATE; ZINC; ESCHERICHIA COLI; PROTEUS INCONSTANS
Active strength
3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage43742-190343742-1903-1DDiscontinued by firm2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage43742-190343742-1903-1DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43742-1903LEAKY GUT FORMULA (ALFALFA, GLYCYRRHIZA GLABRA, ALOE, ASTACUS FLUVIATILIS, BERBERIS AQUIFOLIUM, LAC DEFLORATUM, NATRUM CARBONICUM, SACCHARUM OFFICINALE, FEL TAURI, PANCREAS SUIS, PANCREATINUM, FRAGARIA VESCA, ANTIMONIUM CRUDUM, CARBO VEGETABILIS, EUPHORBIUM OFFICINARUM, LYCOPODIUM CLAVATUM, MAGNESIA CARBONICA, ZINCUM METALLICUM, COLIBACILLINUM CUM NATRUM MURIATICUM, PROTEUS (VULGARIS)) LIQUID [DESERET BIOLOGICALS, INC.]2Legacy NDC20210620_2e139e8c-8ebc-4433-8363-bd377cb048ef.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-1903-14374219030130 mL in 1 BOTTLE, DROPPER (43742-1903-1) 30 ml2020-10-232025-12-02NoNoCurrent