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43406-0720-1 : NDC 2026 Code

43406-0720-1 : Arctostaphylos Uva-ursi Leaf, Berberis Vulgaris Root Bark, Boletus Satanas Fruiting Body, Candida Albicans, Lytta Vesicatoria, Equisetum Hyemale Whole, Lachesis Muta Venom, Bos Taurus Ovary, Saccharomyces Cerevisiae, Solidago Virgaurea Flowering Top, Staphisagria Macrosperma Seed ( Urosode )

Additionally :
You can get information about “43406-0720-1” NDC code in 43406-0720-1 in HTML format HTML  |  43406-0720-1 in TXT (Plain Text) format TXT  |  43406-0720-1 in PDF (Portable Document Format) PDF  |  43406-0720-1 in JSON format JSON  formats.

NDC Code : 43406-0720-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43406-0720-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43406-0720-1) 
	</PackageDescription>
	<NDC11Code>
		43406-0720-01
	</NDC11Code>
	<ProductNDC>
		43406-0720
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Urosode
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Arctostaphylos Uva-ursi Leaf, Berberis Vulgaris Root Bark, Boletus Satanas Fruiting Body, Candida Albicans, Lytta Vesicatoria, Equisetum Hyemale Whole, Lachesis Muta Venom, Bos Taurus Ovary, Saccharomyces Cerevisiae, Solidago Virgaurea Flowering Top, Staphisagria Macrosperma Seed
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20261015
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Natural Creations, Inc
	</LabelerName>
	<SubstanceName>
		ARCTOSTAPHYLOS UVA-URSI LEAF; BERBERIS VULGARIS ROOT BARK; BOLETUS SATANAS FRUITING BODY; CANDIDA ALBICANS; LYTTA VESICATORIA; EQUISETUM HYEMALE WHOLE; LACHESIS MUTA VENOM; BOS TAURUS OVARY; SACCHAROMYCES CEREVISIAE; SOLIDAGO VIRGAUREA FLOWERING TOP; STAPHISAGRIA MACROSPERMA SEED
	</SubstanceName>
	<StrengthNumber>
		12; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30
	</StrengthNumber>
	<StrengthUnit>
		[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2026-10-24
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20271231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20261015
	</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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