MYCCombination

Product NDC
43742-2108
11-digit product format
437422108
Labeler code
43742
Product ID
43742-2108_7b6d8d8f-1d4c-478f-930b-a7aee4633475
Type
HUMAN OTC DRUG
Nonproprietary name
Allium Cepa, Echinacea (Echinacea Angustifolia), Natrum Sulphuricum, Kali Carbonicum, Sanguinaria Canadensis, Agaricus Muscarius, Antimonium Tartaricum, Arsenicum Iodatum, Carbolicum Acidum, Cinchona Officinalis, Ferrum Metallicum, Phytolacca Decandra, Secale Cornutum, Sulphuricum Acidum, Thuja Occidentalis, Ammonium Carbonicum, Aspergillus Niger, Blatta Orientalis, Mephitis Mephitica
Dosage form
LIQUID
Route
ORAL
Labeler
Deseret Biologicals, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-12-20
Marketing end
2029-10-31
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
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
DIF093I037AMANITA MUSCARIA FRUITING BODYAMANITA MUSCARIA FRUITING BODY
NJ5VT0FKLJAMMONIUM CARBONATE8000-73-5AMMONIUM CARBONATE
DL6OZ476V3ANTIMONY POTASSIUM TARTRATE28300-74-5ANTIMONY POTASSIUM TARTRATE
3029988O2TARSENIC TRIIODIDE7784-45-4ARSENIC TRIIODIDE
9IOA40ANG6ASPERGILLUS NIGER VAR. NIGERASPERGILLUS NIGER VAR. NIGER
535787266DBLATTA ORIENTALISBLATTA ORIENTALIS
S003A158SBCINCHONA OFFICINALIS BARKCINCHONA OFFICINALIS BARK
01G9XEA93NCLAVICEPS PURPUREA SCLEROTIUMCLAVICEPS PURPUREA SCLEROTIUM
E1UOL152H7IRON7439-89-6IRON
3BN57UN4USMEPHITIS MEPHITIS ANAL GLAND FLUIDMEPHITIS MEPHITIS ANAL GLAND FLUID
492225Q21HONIONONION
339NCG44TVPHENOL108-95-2PHENOL
11E6VI8VEGPHYTOLACCA AMERICANA ROOTPHYTOLACCA AMERICANA ROOT
BQN1B9B9HAPOTASSIUM CARBONATE584-08-7POTASSIUM CARBONATE
N9288CD508SANGUINARIA CANADENSIS ROOTSANGUINARIA CANADENSIS ROOT
0YPR65R21JSODIUM SULFATE7727-73-3SODIUM SULFATE
O40UQP6WCFSULFURIC ACID7664-93-9SULFURIC ACID
1NT28V9397THUJA OCCIDENTALIS LEAFY TWIGTHUJA OCCIDENTALIS LEAFY TWIG

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
43742-2108-14374221080130 mL in 1 BOTTLE, DROPPER (43742-2108-1) 30 ml2023-12-202029-10-31NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DRUG FACTS:Deseret Biologicals, Inc. | Apotheca Company2025-05-27HUMAN OTC DRUG LABEL3