82969-6007-1 : NDC 2025 Code

82969-6007-1 : Calcarea Phosphorica, Aconite Nap, Anacardium Ori, Argentum Nit, Arsenic Alb, Aurum Mur, Chamomilla, Duboisia, Gelsemium, Ignatia, Kali Brom, Lachesis Mutus, Lycopodium, Mag Mur, Moschus, Nat Carb, Nat Sulph, Phosphoric Acid, Rauwolfia Serp ( Bestmade Natural Products Restful Legs Support )

NDC Code : 82969-6007-1 – XML Data Format

                    
<?xml version="1.0" encoding="UTF-8"?>
<NDC>
	<NDCCode>
		82969-6007-1
	</NDCCode>
	<PackageDescription>
		100 [hp_C] in 1 BOTTLE, GLASS (82969-6007-1) 
	</PackageDescription>
	<NDC11Code>
		82969-6007-01
	</NDC11Code>
	<ProductNDC>
		82969-6007
	</ProductNDC>
	<ProductTypeName>
		HUMAN OTC DRUG
	</ProductTypeName>
	<ProprietaryName>
		Bestmade Natural Products Restful Legs Support
	</ProprietaryName>
	<ProprietaryNameSuffix/>
	<NonProprietaryName>
		Calcarea Phosphorica, Aconite Nap, Anacardium Ori, Argentum Nit, Arsenic Alb, Aurum Mur, Chamomilla, Duboisia, Gelsemium, Ignatia, Kali Brom, Lachesis Mutus, Lycopodium, Mag Mur, Moschus, Nat Carb, Nat Sulph, Phosphoric Acid, Rauwolfia Serp
	</NonProprietaryName>
	<DosageFormName>
		TABLET, SOLUBLE
	</DosageFormName>
	<RouteName>
		ORAL
	</RouteName>
	<StartMarketingDate>
		20150101
	</StartMarketingDate>
	<EndMarketingDate/>
	<MarketingCategoryName>
		UNAPPROVED HOMEOPATHIC
	</MarketingCategoryName>
	<ApplicationNumber/>
	<LabelerName>
		Bestmade Natural Products
	</LabelerName>
	<SubstanceName>
		ACONITUM NAPELLUS; ARSENIC TRIOXIDE; DUBOISIA MYOPOROIDES LEAF; GELSEMIUM SEMPERVIRENS ROOT; GOLD TRICHLORIDE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM CHLORIDE; MATRICARIA CHAMOMILLA; MOSCHUS MOSCHIFERUS MUSK SAC RESIN; PHOSPHORIC ACID; POTASSIUM BROMIDE; RAUWOLFIA SERPENTINA; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; SODIUM CARBONATE; SODIUM SULFATE; STRYCHNOS IGNATII SEED; TRIBASIC CALCIUM PHOSPHATE
	</SubstanceName>
	<StrengthNumber>
		100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100; 100
	</StrengthNumber>
	<StrengthUnit>
		[hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]; [hp_C]/100[hp_C]
	</StrengthUnit>
	<Pharm_Classes>
		Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
	</Pharm_Classes>
	<DEASchedule/>
	<Status>
		Active
	</Status>
	<LastUpdate>
		2025-03-17
	</LastUpdate>
	<PackageNdcExcludeFlag>
		N
	</PackageNdcExcludeFlag>
	<ProductNdcExcludeFlag>
		N
	</ProductNdcExcludeFlag>
	<ListingRecordCertifiedThrough>
		20261231
	</ListingRecordCertifiedThrough>
	<StartMarketingDatePackage>
		20150101
	</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>