43742-2242-1 : NDC 2025 Code

43742-2242-1 : Beta Vulgaris, Boldo, Calcarea Fluorica, Calcarea Phosphorica, Carduus Benedictus, Chelidonium Majus, Coffea Tosta, Equisetum Arvense, Germanium Sesquioxide, Ginkgo Biloba, Hypericum Perforatum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Petroselinum Sativum, Silicea, Taraxacum Officinale ( Hydration Complex )

NDC Code : 43742-2242-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2242-1
	</NDCCode>
	<PackageDescription>
		60 mL in 1 BOTTLE, DROPPER (43742-2242-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2242-01
	</NDC11Code>
	<ProductNDC>
		43742-2242
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Hydration Complex
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Beta Vulgaris, Boldo, Calcarea Fluorica, Calcarea Phosphorica, Carduus Benedictus, Chelidonium Majus, Coffea Tosta, Equisetum Arvense, Germanium Sesquioxide, Ginkgo Biloba, Hypericum Perforatum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Petroselinum Sativum, Silicea, Taraxacum Officinale
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20250116
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		BETA VULGARIS WHOLE; CALCIUM FLUORIDE; CENTAUREA BENEDICTA; CHELIDONIUM MAJUS WHOLE; COFFEA ARABICA SEED, ROASTED; DIBASIC POTASSIUM PHOSPHATE; EQUISETUM ARVENSE TOP; GERMANIUM SESQUIOXIDE; GINKGO; HYPERICUM PERFORATUM WHOLE; PETROSELINUM CRISPUM WHOLE; PEUMUS BOLDUS LEAF; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SILICON DIOXIDE; TARAXACUM OFFICINALE; TRIBASIC CALCIUM PHOSPHATE
	</SubstanceName>
	<StrengthNumber>
		1; 8; 1; 1; 1; 6; 1; 8; 6; 3; 1; 1; 6; 6; 8; 1; 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>
		Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2025-01-18
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20250116
	</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>