43742-2542-1 : NDC 2026 Code

43742-2542-1 : Aconitum Napellus, Adrenalinum, Ambra Grisea, Aurum Muriaticum Natronatum, Calcarea Sulphurica, Cimicifuga Racemosa, Cinchona Officinalis, Cortisone Aceticum, Crocus Sativus, Dna, Hyoscyamus Niger, Hypophysis Suis, Hypothalamus Suis, Ignatia Amara, Kali Bromatum, Lachesis Mutus, Pulsatilla (pratensis), Thyroidinum (bovine), Viola Odorata ( Emotional Detox And Drainage )

NDC Code : 43742-2542-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2542-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43742-2542-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2542-01
	</NDC11Code>
	<ProductNDC>
		43742-2542
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Emotional Detox And Drainage
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Aconitum Napellus, Adrenalinum, Ambra Grisea, Aurum Muriaticum Natronatum, Calcarea Sulphurica, Cimicifuga Racemosa, Cinchona Officinalis, Cortisone Aceticum, Crocus Sativus, Dna, Hyoscyamus Niger, Hypophysis Suis, Hypothalamus Suis, Ignatia Amara, Kali Bromatum, Lachesis Mutus, Pulsatilla (pratensis), Thyroidinum (bovine), Viola Odorata
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20260320
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		ACONITUM NAPELLUS WHOLE; AMBERGRIS; BLACK COHOSH; CALCIUM SULFATE ANHYDROUS; CINCHONA OFFICINALIS BARK; CORTISONE ACETATE; EPINEPHRINE; HERRING SPERM DNA; HYOSCYAMUS NIGER; LACHESIS MUTA VENOM; POTASSIUM BROMIDE; PULSATILLA PRATENSIS WHOLE; SAFFRON; SODIUM TETRACHLOROAURATE; STRYCHNOS IGNATII SEED; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PITUITARY GLAND; THYROID, BOVINE; VIOLA ODORATA WHOLE
	</SubstanceName>
	<StrengthNumber>
		6; 6; 6; 6; 6; 8; 12; 16; 6; 12; 6; 6; 6; 15; 6; 8; 8; 8; 8
	</StrengthNumber>
	<StrengthUnit>
		[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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Blood Coagulation Factor [EPC], Calcium [CS], Catecholamine [EPC], Catecholamines [CS], Cations, Divalent [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2026-03-23
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20271231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20260320
	</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>