Leaky Gut Formula
- Product NDC
- 43742-1535
- Requested package NDC
- 43742-1535-1
- 11-digit product format
- 437421535
- Labeler code
- 43742
- Product ID
- 43742-1535_89f9a0e3-575a-4cb3-ac45-328a64d3f02d
- 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
- 2019-08-22
- Marketing end
- 2025-05-05
- Substance
- ALFALFA; GLYCYRRHIZA GLABRA; ALOE; ASTACUS ASTACUS; BERBERIS AQUIFOLIUM ROOT BARK; SKIM MILK; SODIUM CARBONATE; SUCROSE; BOS TAURUS BILE; SUS SCROFA PANCREAS; PANCRELIPASE; ALPINE STRAWBERRY; ANTIMONY TRISULFIDE; ACTIVATED CHARCOAL; EUPHORBIA RESINIFERA RESIN; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CARBONATE; ZINC; ESCHERICHIA COLI; PROTEUS VULGARIS
- 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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 43742-1535 | 43742-1535-1 | D | Discontinued by firm | 2026-10-05 |
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.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 43742-1535 | 43742-1535-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 43742-1535 | 43742-1535-1 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 43742-1535-1 | 43742153501 | 30 mL in 1 BOTTLE, DROPPER (43742-1535-1) | 30 ml | 2019-08-22 | 2025-05-05 | No | No | Current |