43742-2108 NDC - MYCCOMBINATION (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)

Drug Information

Product NDC: 43742-2108
Proprietary Name: MYCCombination
Non Proprietary 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
Active Ingredient(s): 12 [hp_X]/mL AMANITA MUSCARIA FRUITING BODY; 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 CINCHONA OFFICINALIS BARK; 12 [hp_X]/mL CLAVICEPS PURPUREA SCLEROTIUM; 6 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 12 [hp_X]/mL IRON; 12 [hp_C]/mL MEPHITIS MEPHITIS ANAL GLAND FLUID; 6 [hp_X]/mL ONION; 12 [hp_X]/mL PHENOL; 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 8 [hp_X]/mL POTASSIUM CARBONATE; 8 [hp_X]/mL SANGUINARIA CANADENSIS ROOT; 6 [hp_X]/mL SODIUM SULFATE; 12 [hp_X]/mL SULFURIC ACID; 12 [hp_X]/mL THUJA OCCIDENTALIS LEAFY TWIG
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): 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]

Labeler Information

Field Name	Field Value
Labeler Name:	Deseret Biologicals, Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	12/20/2023
End Marketing Date:	10/31/2029

Package Information

No.	Package Code	Package Description	Billing Unit
1	43742-2108-1	30 mL in 1 BOTTLE, DROPPER (43742-2108-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	43742-2108	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAME	MYCCombination	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY 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	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	LIQUID	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	12/20/2023	This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE	10/31/2029	This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Deseret Biologicals, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	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	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	12; 12; 12; 12; 15; 9; 12; 12; 6; 12; 12; 6; 12; 12; 8; 8; 6; 12; 12
ACTIVE INGRED UNIT	[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
PHARM 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]

Drug Information

Labeler Information

Package Information

NDC Record

Download Record