Home NDC 43742-2291 Mold Plus
Product NDC 43742-2291
11-digit product format 437422291
Labeler code 43742
Product ID 43742-2291_ea9e106e-e338-47d4-add3-0ce3a54503cc
Type HUMAN OTC DRUG
Nonproprietary name Agaricus Muscarius, Allium Cepa, Ammonium Carbonicum, Antimonium Tartaricum, Arsenicum Iodatum, Aspergillus Niger, Blatta Orientalis, Carbolicum Acidum, Cinchona Officinalis, Echinacea (Angustifolia), Ferrum Metallicum, Kali Carbonicum, Mephitis Mephitica, Natrum Sulphuricum, Phytolacca Decandra, Sanguinaria Canadensis, Secale Cornutum, Sulphuricum Acidum, Thuja Occidentalis
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-02-23
Substance AMANITA MUSCARIA FRUITING BODY; AMMONIUM CARBONATE; ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIIODIDE; ASPERGILLUS NIGER VAR. NIGER; BLATTA ORIENTALIS; CINCHONA OFFICINALIS BARK; CLAVICEPS PURPUREA SCLEROTIUM; ECHINACEA ANGUSTIFOLIA WHOLE; IRON; MEPHITIS MEPHITIS ANAL GLAND FLUID; ONION; PHENOL; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE; SANGUINARIA CANADENSIS ROOT; SODIUM SULFATE; SULFURIC ACID; THUJA OCCIDENTALIS LEAFY TWIG
Active strength 12; 12; 12; 12; 15; 9; 12; 12; 6; 12; 12; 6; 12; 12; 8; 8; 6; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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
Pharmacologic classes Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Insect Allergenic Extract [EPC], Vegetable Proteins [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Mold Plus
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength AMANITA MUSCARIA FRUITING BODY 12 [hp_X]/mL ONION 12 [hp_X]/mL AMMONIUM CARBONATE 12 [hp_X]/mL ANTIMONY POTASSIUM TARTRATE 12 [hp_X]/mL ARSENIC TRIIODIDE 15 [hp_X]/mL ASPERGILLUS NIGER VAR. NIGER 9 [hp_C]/mL BLATTA ORIENTALIS 12 [hp_X]/mL PHENOL 12 [hp_X]/mL CINCHONA OFFICINALIS BARK 6 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE 12 [hp_X]/mL IRON 12 [hp_C]/mL POTASSIUM CARBONATE 6 [hp_X]/mL MEPHITIS MEPHITIS ANAL GLAND FLUID 12 [hp_X]/mL SODIUM SULFATE 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT 8 [hp_X]/mL SANGUINARIA CANADENSIS ROOT 8 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM 6 [hp_X]/mL SULFURIC ACID 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 19 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-2291-1 Mold Plus 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Mold Plus AGARICUS MUSCARIUS, ALLIUM CEPA, AMMONIUM CARBONICUM, ANTIMONIUM TARTARICUM, ARSENICUM IODATUM, ASPERGILLUS NIGER, BLATTA ORIENTALIS, CARBOLICUM ACIDUM, CINCHONA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), FERRUM METALLICUM, KALI CARBONICUM, MEPHITIS MEPHITICA, NATRUM SULPHURICUM, PHYTOLACCA DECANDRA, SANGUINARIA CANADENSIS, SECALE CORNUTUM, SULPHURICUM ACIDUM, THUJA OCCIDENTALIS Deseret Biologicals, Inc. 372ad9cc-70eb-4f3f-b611-69e2d157c058 2026-02-23 Warnings Exact identifier ndc (product): 43742-2291
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 43742-2291-1 43742229101 30 mL in 1 BOTTLE, DROPPER (43742-2291-1) 30 ml 2026-02-23 No No Current