43742-2549-1 : NDC 2026 Code

43742-2549-1 : Acetaldehyde, Alfalfa, Alpha-ketoglutaricum Acidum, Alpha-lipoicum Acidum, Ascorbyl Palmitate, Cobaltum Metallicum, Cysteinum, Dimethyl Glycine, Ferrum Metallicum, Fucus Vesiculosus, Gaba (gamma Aminobutyric Acid), Glutathione, Hordeum Vulgare, L-methionine, Magnesium Fluoratum, Manganese Gluconate, Nasturtium Aquaticum, Oryza Sativa, Quercetin, Raphanus Sativus, Selenium Metallicum, Sodium Selenite, Triticum Aestivum, Ubidecarenonum, Vitamin E, Zinc Picolinate, Zincum Metallicum ( Free Radical )

NDC Code : 43742-2549-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2549-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43742-2549-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2549-01
	</NDC11Code>
	<ProductNDC>
		43742-2549
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Free Radical
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Acetaldehyde, Alfalfa, Alpha-ketoglutaricum Acidum, Alpha-lipoicum Acidum, Ascorbyl Palmitate, Cobaltum Metallicum, Cysteinum, Dimethyl Glycine, Ferrum Metallicum, Fucus Vesiculosus, Gaba (gamma Aminobutyric Acid), Glutathione, Hordeum Vulgare, L-methionine, Magnesium Fluoratum, Manganese Gluconate, Nasturtium Aquaticum, Oryza Sativa, Quercetin, Raphanus Sativus, Selenium Metallicum, Sodium Selenite, Triticum Aestivum, Ubidecarenonum, Vitamin E, Zinc Picolinate, Zincum Metallicum
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20260602
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		.ALPHA.-TOCOPHEROL; .GAMMA.-AMINOBUTYRIC ACID; ACETALDEHYDE; ALPHA LIPOIC ACID; ASCORBYL PALMITATE; BROWN RICE; COBALT; CYSTEINE; FUCUS VESICULOSUS; GLUTATHIONE; HORDEUM VULGARE TOP; IRON; MAGNESIUM FLUORIDE; MANGANESE GLUCONATE, UNSPECIFIED FORM; MEDICAGO SATIVA WHOLE; METHIONINE; N,N-DIMETHYLGLYCINE; NASTURTIUM OFFICINALE; OXOGLURIC ACID; QUERCETIN; RADISH; SELENIUM; SODIUM SELENITE; TRITICUM AESTIVUM WHOLE; UBIDECARENONE; ZINC; ZINC PICOLINATE
	</SubstanceName>
	<StrengthNumber>
		8; 8; 30; 8; 6; 8; 12; 6; 12; 12; 6; 12; 30; 6; 6; 6; 6; 6; 30; 6; 6; 12; 6; 6; 6; 12; 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; [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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Dietary Proteins [CS], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2026-06-03
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20271231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20260602
	</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>