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43742-2569-1 : NDC 2026 Code

43742-2569-1 : Acetone, Arsenicum Album, Benzinum, Berberis Vulgaris, Cadmium Sulphuratum, Carbon Dioxide, Carboneum Sulphuratum, Chlorinum, Hydrofluoricum Acidum, Melatonin, Mercurius Solubilis, Nitrogenum Oxygenatum, Nux Vomica, Ozone, Petroleum, Plumbum Metallicum, Stannum Metallicum, Sulphuricum Acidum, Toluene, Uranium Nitricum ( Pollutox )

Additionally :
You can get information about “43742-2569-1” NDC code in 43742-2569-1 in HTML format HTML  |  43742-2569-1 in TXT (Plain Text) format TXT  |  43742-2569-1 in PDF (Portable Document Format) PDF  |  43742-2569-1 in JSON format JSON  formats.

NDC Code : 43742-2569-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2569-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43742-2569-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2569-01
	</NDC11Code>
	<ProductNDC>
		43742-2569
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Pollutox
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Acetone, Arsenicum Album, Benzinum, Berberis Vulgaris, Cadmium Sulphuratum, Carbon Dioxide, Carboneum Sulphuratum, Chlorinum, Hydrofluoricum Acidum, Melatonin, Mercurius Solubilis, Nitrogenum Oxygenatum, Nux Vomica, Ozone, Petroleum, Plumbum Metallicum, Stannum Metallicum, Sulphuricum Acidum, Toluene, Uranium Nitricum
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20260909
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		ACETONE; ARSENIC TRIOXIDE; BENZENE; BERBERIS VULGARIS ROOT BARK; CADMIUM SULFIDE; CARBON DIOXIDE; CARBON DISULFIDE; CHLORINE; HYDROFLUORIC ACID; MELATONIN; MERCURIUS SOLUBILIS; NITROUS OXIDE; STRYCHNOS NUX-VOMICA SEED; OZONE; LIQUID PETROLEUM; LEAD; TIN; SULFURIC ACID; TOLUENE; URANYL NITRATE HEXAHYDRATE
	</SubstanceName>
	<StrengthNumber>
		12; 12; 12; 8; 12; 15; 12; 12; 16; 12; 12; 12; 12; 16; 12; 12; 12; 6; 12; 15
	</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_C]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Radiographic Contrast Agent [EPC], Seed Storage Proteins [CS], X-Ray Contrast Activity [MoA]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2026-09-11
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20271231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20260909
	</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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