43742-2259 NDC - BIO CO ENZYME PHASE (ACONITICUM ACIDUM, CIS-, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ADRENALINUM, , ALPHA-KETOGLUTARICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, ASCORBICUM ACIDUM, BARIUM OXALSUCCINICUM, BETA VULGARIS, CERIUM OXALICUM, CITRICUM ACIDUM, CYSTEINUM, FUMARICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, MAGNESIUM OROTICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM PHOSPHORICUM, NADIDUM, NATRUM OXALACETICUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PANTOTHENIC ACID, PROTEUS (MORGANI), PULSATILLA (PRATENSIS), PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM,)

Drug Information

  • Product NDC: 43742-2259
  • Proprietary Name: Bio Co Enzyme Phase
  • Non Proprietary Name: Aconiticum Acidum, Cis-, Adenosinum Triphosphoricum Dinatrum, Adrenalinum, , Alpha-Ketoglutaricum Acidum, Alpha-Lipoicum Acidum, Ascorbicum Acidum, Barium Oxalsuccinicum, Beta Vulgaris, Cerium Oxalicum, Citricum Acidum, Cysteinum, Fumaricum Acidum, Hepar Sulphuris Calcareum, Magnesium Oroticum Dihydricum, Malicum Acidum, Manganum Phosphoricum, Nadidum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pantothenic Acid, Proteus (Morgani), Pulsatilla (Pratensis), Pyridoxinum Hydrochloricum, Riboflavinum,
  • Active Ingredient(s): 16 [hp_X]/mL ACONITIC ACID; 10 [hp_X]/mL ADENOSINE TRIPHOSPHATE DISODIUM; 8 [hp_X]/mL ALPHA LIPOIC ACID; 8 [hp_X]/mL ANHYDROUS CITRIC ACID; 6 [hp_X]/mL ASCORBIC ACID; 34 [hp_C]/mL BARIUM OXALOSUCCINATE; 4 [hp_X]/mL BETA VULGARIS WHOLE; 16 [hp_X]/mL CALCIUM SULFIDE; 8 [hp_X]/mL CEROUS OXALATE NONAHYDRATE; 6 [hp_X]/mL CYSTEINE; 8 [hp_X]/mL EPINEPHRINE; 8 [hp_X]/mL FUMARIC ACID; 8 [hp_X]/mL MAGNESIUM OROTATE DIHYDRATE; 8 [hp_X]/mL MALIC ACID; 16 [hp_X]/mL MANGANESE PHOSPHATE, DIBASIC; 8 [hp_X]/mL NADIDE; 6 [hp_X]/mL NIACINAMIDE; 8 [hp_X]/mL OXOGLURIC ACID; 8 [hp_X]/mL PANTOTHENIC ACID; 30 [hp_C]/mL PROTEUS MORGANII; 6 [hp_X]/mL PULSATILLA PRATENSIS WHOLE; 6 [hp_X]/mL PYRIDOXINE HYDROCHLORIDE; 6 [hp_X]/mL RIBOFLAVIN; 6 [hp_X]/mL SODIUM DIETHYL OXALACETATE; 8 [hp_X]/mL SODIUM PYRUVATE; 8 [hp_X]/mL SUCCINIC ACID; 10 [hp_X]/mL SULFUR; 6 [hp_X]/mL THIAMINE HYDROCHLORIDE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Acidifying Activity [MoA]; Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Analogs/Derivatives [Chemical/Ingredient]; Anti-coagulant [EPC]; Ascorbic Acid [CS]; Calcium Chelating Activity [MoA]; Calculi Dissolution Agent [EPC]; Catecholamine [EPC]; Catecholamines [CS]; Decreased Coagulation Factor Activity [PE]; Magnetic Resonance Contrast Activity [MoA]; Paramagnetic Contrast Agent [EPC]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

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:4/8/2025

Package Information

No. Package Code Package Description Billing Unit
143742-2259-130 mL in 1 BOTTLE, DROPPER (43742-2259-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2259The 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 NAMEHUMAN OTC DRUGIndicates 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 NAMEBio Co Enzyme PhaseThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAconiticum Acidum, Cis-, Adenosinum Triphosphoricum Dinatrum, Adrenalinum, , Alpha-Ketoglutaricum Acidum, Alpha-Lipoicum Acidum, Ascorbicum Acidum, Barium Oxalsuccinicum, Beta Vulgaris, Cerium Oxalicum, Citricum Acidum, Cysteinum, Fumaricum Acidum, Hepar Sulphuris Calcareum, Magnesium Oroticum Dihydricum, Malicum Acidum, Manganum Phosphoricum, Nadidum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pantothenic Acid, Proteus (Morgani), Pulsatilla (Pratensis), Pyridoxinum Hydrochloricum, Riboflavinum,The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/8/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; ALPHA LIPOIC ACID; ANHYDROUS CITRIC ACID; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BETA VULGARIS WHOLE; CALCIUM SULFIDE; CEROUS OXALATE NONAHYDRATE; CYSTEINE; EPINEPHRINE; FUMARIC ACID; MAGNESIUM OROTATE DIHYDRATE; MALIC ACID; MANGANESE PHOSPHATE, DIBASIC; NADIDE; NIACINAMIDE; OXOGLURIC ACID; PANTOTHENIC ACID; PROTEUS MORGANII; PULSATILLA PRATENSIS WHOLE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; SUCCINIC ACID; SULFUR; THIAMINE HYDROCHLORIDEAn 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 STRENGTH16; 10; 8; 8; 6; 34; 4; 16; 8; 6; 8; 8; 8; 8; 16; 8; 6; 8; 8; 30; 6; 6; 6; 6; 8; 8; 10; 6 
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_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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAcidifying Activity [MoA], Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Analogs/Derivatives [Chemical/Ingredient], Anti-coagulant [EPC], Ascorbic Acid [CS], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Catecholamine [EPC], Catecholamines [CS], Decreased Coagulation Factor Activity [PE], Magnetic Resonance Contrast Activity [MoA], Paramagnetic Contrast Agent [EPC], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC], Vitamin C [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

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This page was last updated on: 5/26/2025

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