Grain and Soy Allergen Mix
- Product NDC
- 43742-1417
- Requested package NDC
- 43742-1417-1
- 11-digit product format
- 437421417
- Labeler code
- 43742
- Product ID
- 43742-1417_55a863d0-8ea2-48d1-aaea-b227e53c5eed
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Adenosinum Triphosphoricum Dinatrum, Quercetin, Rutin, Ileum (Suis), Jejunum (Suis) Stomach (Suis), Bamboo, Barley, Poppy Seed, Corn, Flax Seed, Cotton Seed, Millet, Milo, Oat, Rice, Rye, Safflower, Sesame, Sorghum, Soy Bean, Sugarcane, Sunflower, Wheat, Bacillus Thuringiensis (BT Toxin), Gluten, Amaranth, Avena Sativa, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Glyphosate, Sycotic Co Bacillus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2019-01-02
- Marketing end
- 2025-02-25
- Substance
- ADENOSINE TRIPHOSPHATE DISODIUM; QUERCETIN; RUTIN; SUS SCROFA ILEUM; SUS SCROFA JEJUNUM; SUS SCROFA STOMACH; BAMBUSA VULGARIS LEAF; BARLEY; POPPY SEED; CORN; FLAX SEED; LEVANT COTTON SEED; MILLET; SORGHUM BICOLOR WHOLE; OAT; BROWN RICE; RYE; SAFFLOWER; SESAME SEED; SORGHUM; SOYBEAN; SUGARCANE; SUNFLOWER SEED; WHEAT; BACILLUS THURINGIENSIS; WHEAT GLUTEN; AMARANTH; AVENA SATIVA FLOWERING TOP; SODIUM SULFATE; LACTIC ACID, L-; ELYMUS REPENS ROOT; CORTICOTROPIN; GLYPHOSATE; ENTEROCOCCUS FAECALIS
- Active strength
- 4 [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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- DEA schedule
- CII
- 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 | 43742-1417 | 43742-1417-1 | 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 | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
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 |
|---|---|---|---|---|---|---|---|---|
| 43742-1417-1 | 43742141701 | 30 mL in 1 BOTTLE, DROPPER (43742-1417-1) | 30 ml | 2019-01-02 | 2025-02-25 | No | No | Current |