55146-006-01 : NDC 2026 Code

55146-006-01 : Baptisia Tinctoria, Phytolacca Decandra, Spigelia Anthelmia, Adrenocorticotrophin, Aluminum Metallicum, Apis Mellifica, Argentum Nitricum, Arsenicum Album, Benzoicum Acidum, Calcarea Carbonica, Carbo Vegetabilis, Kali Phosphoricum, Magnesia Sulphurica, Mercurius Solubilis, Nitricum Acidum, Nux Vomica, Phosphorus, Silicea ( 6 Environmental Detox )

NDC Code : 55146-006-01 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		55146-006-01
	</NDCCode>
	<PackageDescription>
		120 mL in 1 BOTTLE, PLASTIC (55146-006-01) 
	</PackageDescription>
	<NDC11Code>
		55146-0006-01
	</NDC11Code>
	<ProductNDC>
		55146-006
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		6 Environmental Detox
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Baptisia Tinctoria, Phytolacca Decandra, Spigelia Anthelmia, Adrenocorticotrophin, Aluminum Metallicum, Apis Mellifica, Argentum Nitricum, Arsenicum Album, Benzoicum Acidum, Calcarea Carbonica, Carbo Vegetabilis, Kali Phosphoricum, Magnesia Sulphurica, Mercurius Solubilis, Nitricum Acidum, Nux Vomica, Phosphorus, Silicea
	</NonProprietaryName>
	<DosageFormName>
		LIQUID
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20190611
	</StartMarketingDate>
	<EndMarketingDate>
		20251211
	</EndMarketingDate>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Biotics Research Corporation
	</LabelerName>
	<SubstanceName>
		ACTIVATED CHARCOAL; ALUMINUM; APIS MELLIFERA; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BENZOIC ACID; CORTICOTROPIN; MAGNESIUM SULFATE HEPTAHYDRATE; MERCURIUS SOLUBILIS; NITRIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM PHOSPHATE, DIBASIC; SILICON DIOXIDE; SILVER NITRATE; SPIGELIA ANTHELMIA WHOLE; STRYCHNOS NUX-VOMICA SEED
	</SubstanceName>
	<StrengthNumber>
		30; 30; 30; 30; 3; 30; 30; 30; 30; 30; 30; 30; 4; 30; 30; 30; 6; 30
	</StrengthNumber>
	<StrengthUnit>
		[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL
	</StrengthUnit>
	<Pharm_Classes>
		Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Nitrogen Binding Agent [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Deprecated
	</Status>
	<LastUpdate>
		2025-12-16
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough/>
	<StartMarketingDatePackage>
		20190611
	</StartMarketingDatePackage>
	<EndMarketingDatePackage>
		20251211
	</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>