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50181-0069-1 : NDC 2025 Code

50181-0069-1 : Lycopodium Clavatum, Abies Canadensis, Ammonium Bromatum, Ammonium Muriaticum, Phytolacca Decandra, Pulsatilla (pratensis), Ammonium Carbonicum, Fucus Vesiculosus, Capsicum Annuum, Argentum Nitricum, Kali Bichromicum, Silicea, Glandula Suprarenalis Bovine, Calcarea Arsenicica, Ferrum Metallicum, Antimonium Crudum, Calcarea Carbonica, Graphites, Kali Carbonicum, Anacardium Orientale, Iodium, Thyroidinum (suis), Leptin ( Slim )

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You can get information about “50181-0069-1” NDC code in 50181-0069-1 in HTML format HTML  |  50181-0069-1 in TXT (Plain Text) format TXT  |  50181-0069-1 in PDF (Portable Document Format) PDF  |  50181-0069-1 in JSON format JSON  formats.

NDC Code : 50181-0069-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		50181-0069-1
	</NDCCode>
	<PackageDescription>
		30 mL in 1 BOTTLE, DROPPER (50181-0069-1) 
	</PackageDescription>
	<NDC11Code>
		50181-0069-01
	</NDC11Code>
	<ProductNDC>
		50181-0069
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Slim
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Lycopodium Clavatum, Abies Canadensis, Ammonium Bromatum, Ammonium Muriaticum, Phytolacca Decandra, Pulsatilla (pratensis), Ammonium Carbonicum, Fucus Vesiculosus, Capsicum Annuum, Argentum Nitricum, Kali Bichromicum, Silicea, Glandula Suprarenalis Bovine, Calcarea Arsenicica, Ferrum Metallicum, Antimonium Crudum, Calcarea Carbonica, Graphites, Kali Carbonicum, Anacardium Orientale, Iodium, Thyroidinum (suis), Leptin
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20200309
	</StartMarketingDate>
	<EndMarketingDate>
		20281028
	</EndMarketingDate>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		The Wellness Center for Research and Education
	</LabelerName>
	<SubstanceName>
		AMMONIUM BROMIDE; AMMONIUM CARBONATE; AMMONIUM CHLORIDE; ANTIMONY TRISULFIDE; BOS TAURUS ADRENAL GLAND; CALCIUM ARSENATE; CAPSICUM; FUCUS VESICULOSUS; GRAPHITE; IODINE; IRON; LEPTIN HUMAN; LYCOPODIUM CLAVATUM SPORE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; POTASSIUM CARBONATE; POTASSIUM DICHROMATE; PULSATILLA PRATENSIS WHOLE; SEMECARPUS ANACARDIUM JUICE; SILICON DIOXIDE; SILVER NITRATE; THYROID; TSUGA CANADENSIS BARK
	</SubstanceName>
	<StrengthNumber>
		3; 6; 3; 12; 8; 12; 6; 6; 12; 4; 12; 14; 2; 12; 4; 30; 6; 4; 4; 8; 6; 5; 3
	</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_C]/mL; [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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2025-06-10
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough/>
	<StartMarketingDatePackage>
		20200309
	</StartMarketingDatePackage>
	<EndMarketingDatePackage>
		20281028
	</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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