44911-0725-1 : NDC 2026 Code

44911-0725-1 : Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Butyl Acetate, Ethyl Acetate, Toluene, Xylene, Bisphenol A, Petroleum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Propylparaben, Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla (pratensis), Sulphur, Paraffinum ( Household Antigens )

NDC Code : 44911-0725-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		44911-0725-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (44911-0725-1) 
	</PackageDescription>
	<NDC11Code>
		44911-0725-01
	</NDC11Code>
	<ProductNDC>
		44911-0725
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Household Antigens
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Butyl Acetate, Ethyl Acetate, Toluene, Xylene, Bisphenol A, Petroleum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Propylparaben, Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla (pratensis), Sulphur, Paraffinum
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20241220
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Energique, Inc.
	</LabelerName>
	<SubstanceName>
		ACETONE; AMMONIUM CHLORIDE; BENZENE; BISPHENOL A; BUTYL ACETATE; ETHYL ACETATE; FORMALDEHYDE SOLUTION; GLYPHOSATE; GRAPHITE; KEROSENE; METHYLPARABEN; NAPHTHALENE; NITRIC ACID; PARAFFIN; PROPYLENE GLYCOL; PROPYLPARABEN; PULSATILLA PRATENSIS WHOLE; SEMECARPUS ANACARDIUM JUICE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM; SULFUR; TOLUENE; TURPENTINE OIL; XYLENE (MIXED ISOMERS)
	</SubstanceName>
	<StrengthNumber>
		9; 9; 9; 9; 9; 9; 9; 9; 12; 9; 9; 9; 12; 12; 9; 9; 12; 12; 9; 9; 12; 9; 9; 9
	</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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2024-12-27
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20241220
	</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>