43742-2200-1 : NDC 2025 Code

43742-2200-1 : Aconitum Napellus, Adrenalinum, Agaricus Muscarius, Apis Mellifica, Atropinum, Camphora, Cantharis, Causticum, Cerebrum Suis, Chamomilla, Cicuta Virosa, Cuprum Metallicum, Homarus, Hyoscyamus Niger, Hypophysis Suis, Lac Caninum, Moschus, Stramonium, Tarentula Hispana, Veratrum Album ( Rage )

NDC Code : 43742-2200-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2200-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43742-2200-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2200-01
	</NDC11Code>
	<ProductNDC>
		43742-2200
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Rage
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Aconitum Napellus, Adrenalinum, Agaricus Muscarius, Apis Mellifica, Atropinum, Camphora, Cantharis, Causticum, Cerebrum Suis, Chamomilla, Cicuta Virosa, Cuprum Metallicum, Homarus, Hyoscyamus Niger, Hypophysis Suis, Lac Caninum, Moschus, Stramonium, Tarentula Hispana, Veratrum Album
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20241106
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		ACONITUM NAPELLUS WHOLE; AMANITA MUSCARIA FRUITING BODY; APIS MELLIFERA; ATROPINE; CAMPHOR (NATURAL); CANIS LUPUS FAMILIARIS MILK; CAUSTICUM; CICUTA VIROSA ROOT; COPPER; DATURA STRAMONIUM; EPINEPHRINE; HOMARUS AMERICANUS DIGESTIVE FLUID; HYOSCYAMUS NIGER; LYCOSA TARANTULA; LYTTA VESICATORIA; MATRICARIA CHAMOMILLA WHOLE; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; SUS SCROFA CEREBRUM; SUS SCROFA PITUITARY GLAND; VERATRUM ALBUM ROOT
	</SubstanceName>
	<StrengthNumber>
		12; 12; 6; 12; 30; 12; 12; 12; 12; 12; 8; 17; 12; 16; 6; 6; 12; 8; 8; 12
	</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; [hp_X]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Anticholinergic [EPC], Bee Venoms [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Standardized Insect Venom Allergenic Extract [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2024-11-13
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20241106
	</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>