43742-0652 NDC - PERICARDIUM TRIPLE WARMER (ARSENICUM ALBUM, AURUM METALLICUM, BARYTA CARBONICA, CALCAREA CARBONICA, GLONOINUM, IODIUM, KALI IODATUM, LACHESIS MUTUS, LITHIUM CARBONICUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIA, SPONGIA TOSTA, TABACUM, THYROIDINUM (SUIS))

Drug Information

Product NDC: 43742-0652
Proprietary Name: Pericardium Triple Warmer
Non Proprietary Name: Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Glonoinum, Iodium, Kali Iodatum, Lachesis Mutus, Lithium Carbonicum, Mercurius Solubilis, Naja Tripudians, Phosphoricum Acidum, Phosphorus, Sepia, Spongia Tosta, Tabacum, Thyroidinum (Suis)
Active Ingredient(s): 30 [hp_C]/mL ARSENIC TRIOXIDE; 30 [hp_C]/mL BARIUM CARBONATE; 30 [hp_C]/mL GOLD; 30 [hp_C]/mL IODINE; 30 [hp_C]/mL LACHESIS MUTA VENOM; 30 [hp_C]/mL LITHIUM CARBONATE; 30 [hp_C]/mL MERCURIUS SOLUBILIS; 30 [hp_C]/mL NAJA NAJA VENOM; 30 [hp_C]/mL NITROGLYCERIN; 30 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 30 [hp_C]/mL PHOSPHORIC ACID; 30 [hp_C]/mL PHOSPHORUS; 30 [hp_C]/mL POTASSIUM IODIDE; 30 [hp_C]/mL SEPIA OFFICINALIS JUICE; 30 [hp_C]/mL SPONGIA OFFICINALIS SKELETON, ROASTED; 30 [hp_C]/mL THYROID; 30 [hp_C]/mL TOBACCO LEAF
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Mood Stabilizer [EPC]; Nitrate Vasodilator [EPC]; Nitrates [CS]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Standardized Chemical Allergen [EPC]; Vasodilation [PE]

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:	11/17/2015

Package Information

No.	Package Code	Package Description	Billing Unit
1	43742-0652-1	30 mL in 1 BOTTLE, DROPPER (43742-0652-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	43742-0652	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	Pericardium Triple Warmer	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	Meridian Opener	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAME	Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Calcarea Carbonica, Glonoinum, Iodium, Kali Iodatum, Lachesis Mutus, Lithium Carbonicum, Mercurius Solubilis, Naja Tripudians, Phosphoricum Acidum, Phosphorus, Sepia, Spongia Tosta, Tabacum, Thyroidinum (Suis)	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	11/17/2015	This is the date that the labeler indicates was the start of its marketing of the drug product.
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	ARSENIC TRIOXIDE; BARIUM CARBONATE; GOLD; IODINE; LACHESIS MUTA VENOM; LITHIUM CARBONATE; MERCURIUS SOLUBILIS; NAJA NAJA VENOM; NITROGLYCERIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORIC ACID; PHOSPHORUS; POTASSIUM IODIDE; SEPIA OFFICINALIS JUICE; SPONGIA OFFICINALIS SKELETON, ROASTED; THYROID; TOBACCO LEAF	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	30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30
ACTIVE INGRED UNIT	[hp_C]/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; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
PHARM CLASSES	Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Mood Stabilizer [EPC], Nitrate Vasodilator [EPC], Nitrates [CS], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Vasodilation [PE]

Drug Information

Labeler Information

Package Information

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