43742-2277-1 : NDC 2026 Code

43742-2277-1 : Adrenalinum, Ammonium Muriaticum, Apocynum Cannabinum, Buthus Australis, Carduus Marianus, Cinchona Officinalis, Fel Tauri, Hepar Suis, Hepar Sulphuris Calcareum, Hypothalamus Suis, Manganum Carbonicum, Moschus, Naja Tripudians, Natrum Muriaticum, Nitricum Acidum, Nux Vomica, Rhus Tox, Taraxacum Officinale ( Resentment )

NDC Code : 43742-2277-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		43742-2277-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (43742-2277-1) 
	</PackageDescription>
	<NDC11Code>
		43742-2277-01
	</NDC11Code>
	<ProductNDC>
		43742-2277
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Resentment
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Adrenalinum, Ammonium Muriaticum, Apocynum Cannabinum, Buthus Australis, Carduus Marianus, Cinchona Officinalis, Fel Tauri, Hepar Suis, Hepar Sulphuris Calcareum, Hypothalamus Suis, Manganum Carbonicum, Moschus, Naja Tripudians, Natrum Muriaticum, Nitricum Acidum, Nux Vomica, Rhus Tox, Taraxacum Officinale
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20260226
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Deseret Biologicals, Inc.
	</LabelerName>
	<SubstanceName>
		AMMONIUM CHLORIDE; ANDROCTONUS AUSTRALIS VENOM; APOCYNUM CANNABINUM ROOT; BOS TAURUS BILE; CALCIUM SULFIDE; CINCHONA OFFICINALIS BARK; EPINEPHRINE; MANGANESE CARBONATE; MILK THISTLE; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; NAJA NAJA VENOM; NITRIC ACID; PORK LIVER; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA HYPOTHALAMUS; TARAXACUM OFFICINALE; TOXICODENDRON PUBESCENS LEAF
	</SubstanceName>
	<StrengthNumber>
		6; 12; 12; 12; 12; 12; 12; 12; 6; 12; 12; 6; 8; 6; 12; 8; 6; 12
	</StrengthNumber>
	<StrengthUnit>
		[hp_X]/mL; [hp_C]/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>
		Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Plant Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2026-02-28
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20271231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20260226
	</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>