43742-2259-1 : NDC 2026 Code

43742-2259-1 : 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, ( Bio Co Enzyme Phase )

NDC Code : 43742-2259-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2259-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43742-2259-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2259-01
	</NDC11Code>
	<ProductNDC>
		43742-2259
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Bio Co Enzyme Phase
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		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,
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20250408
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		ACONITIC 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 HYDROCHLORIDE
	</SubstanceName>
	<StrengthNumber>
		16; 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
	</StrengthNumber>
	<StrengthUnit>
		[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
	</StrengthUnit>
	<Pharm_Classes>
		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]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2025-04-10
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20250408
	</StartMarketingDatePackage>
	<EndMarketingDatePackage/>
	<SamplePackage>
		N
	</SamplePackage>
</NDC>

                    
                

NDC XML XSD Schema

                    
<xs:schema attributeFormDefault="unqualified" elementFormDefault="qualified" xmlns:xs="http://www.w3.org/2001/XMLSchema">
  <xs:element name="NDC">
    <xs:complexType>
      <xs:sequence>
        <xs:element type="xs:string" name="NDCCode"/>
        <xs:element type="xs:string" name="PackageDescription"/>
        <xs:element type="xs:string" name="NDC11Code"/>
        <xs:element type="xs:string" name="ProductNDC"/>
        <xs:element type="xs:string" name="ProductTypeName"/>
        <xs:element type="xs:string" name="ProprietaryName"/>
        <xs:element type="xs:string" name="ProprietaryNameSuffix"/>
        <xs:element type="xs:string" name="NonProprietaryName"/>
        <xs:element type="xs:string" name="DosageFormName"/>
        <xs:element type="xs:string" name="RouteName"/>
        <xs:element type="xs:string" name="StartMarketingDate"/>
        <xs:element type="xs:string" name="EndMarketingDate"/>
        <xs:element type="xs:string" name="MarketingCategoryName"/>
        <xs:element type="xs:string" name="ApplicationNumber"/>
        <xs:element type="xs:string" name="LabelerName"/>
        <xs:element type="xs:string" name="SubstanceName"/>
        <xs:element type="xs:string" name="StrengthNumber"/>
        <xs:element type="xs:string" name="StrengthUnit"/>
        <xs:element type="xs:string" name="Pharm_Classes"/>
        <xs:element type="xs:string" name="DEASchedule"/>
        <xs:element type="xs:string" name="Status"/>
        <xs:element type="xs:string" name="LastUpdate"/>
        <xs:element type="xs:string" name="PackageNdcExcludeFlag"/>
        <xs:element type="xs:string" name="ProductNdcExcludeFlag"/>
        <xs:element type="xs:string" name="ListingRecordCertifiedThrough"/>
        <xs:element type="xs:string" name="StartMarketingDatePackage"/>
        <xs:element type="xs:string" name="EndMarketingDatePackage"/>
        <xs:element type="xs:string" name="SamplePackage"/>
      </xs:sequence>
    </xs:complexType>
  </xs:element>
</xs:schema>