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43857-0547-1 : NDC 2025 Code

43857-0547-1 : Echinacea (angustifolia), Tabebuia Impetiginosa, Hydrastis Canadensis, Glandula Suprarenalis Suis, Thymus (suis), Thyroidinum (suis), Arsenicum Album, Bryonia (alba), Cocculus Indicus, Colchicum Autumnale, Ledum Palustre, Mercurius Cyanatus, Natrum Sulphuricum, Pulsatilla (pratensis), Sepia, Silicea, Aflatoxin (b1) ( Asp )

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You can get information about “43857-0547-1” NDC code in 43857-0547-1 in HTML format HTML  |  43857-0547-1 in TXT (Plain Text) format TXT  |  43857-0547-1 in PDF (Portable Document Format) PDF  |  43857-0547-1 in JSON format JSON  formats.

NDC Code : 43857-0547-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43857-0547-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43857-0547-1) 
	</PackageDescription>
	<NDC11Code>
		43857-0547-01
	</NDC11Code>
	<ProductNDC>
		43857-0547
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Asp
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Echinacea (angustifolia), Tabebuia Impetiginosa, Hydrastis Canadensis, Glandula Suprarenalis Suis, Thymus (suis), Thyroidinum (suis), Arsenicum Album, Bryonia (alba), Cocculus Indicus, Colchicum Autumnale, Ledum Palustre, Mercurius Cyanatus, Natrum Sulphuricum, Pulsatilla (pratensis), Sepia, Silicea, Aflatoxin (b1)
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20200303
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		BioActive Nutritional, Inc.
	</LabelerName>
	<SubstanceName>
		AFLATOXIN B1; ANAMIRTA COCCULUS SEED; ARSENIC TRIOXIDE; BRYONIA ALBA ROOT; COLCHICUM AUTUMNALE BULB; ECHINACEA ANGUSTIFOLIA WHOLE; GOLDENSEAL; HANDROANTHUS IMPETIGINOSUS BARK; LEDUM PALUSTRE TWIG; MERCURIC CYANIDE; PULSATILLA PRATENSIS WHOLE; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SODIUM SULFATE; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; THYROID
	</SubstanceName>
	<StrengthNumber>
		30; 12; 12; 12; 12; 3; 5; 3; 12; 12; 12; 12; 12; 12; 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
	</StrengthUnit>
	<Pharm_Classes/>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2024-08-30
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20200303
	</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>
                    
                

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