70719-0003 NDC - HEILEN (GALIUM APARINE, AGNUS CASTUS, APIS MELLIFICA, CAPSICUM ANNUUM, CHELIDONIUM MAJUS, TARAXACUM OFFICINALE, URTICA DIOICA, XANTHOXYLUM FRAXINEUM, FUCUS VESICULOSUS, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, NATRUM PHOSPHORICUM, SARSAPARILLA (SMILAX REGELII), UBIDECARENONUM, CALCAREA CARBONICA, GRAPHITES, LYCOPODIUM CLAVATUM, ANACARDIUM ORIENTALE, COLCHICUM AUTUMNALE, NUX VOMICA, PHYTOLACCA DECANDRA, PULSATILLA (PRATENSIS), HISTAMINUM HYDROCHLORICUM)

Drug Information

Product NDC: 70719-0003

Proprietary Name: Heilen

Non Proprietary Name: Galium Aparine, Agnus Castus, Apis Mellifica, Capsicum Annuum, Chelidonium Majus, Taraxacum Officinale, Urtica Dioica, Xanthoxylum Fraxineum, Fucus Vesiculosus, Kali Phosphoricum, Magnesia Phosphorica, Natrum Phosphoricum, Sarsaparilla (smilax Regelii), Ubidecarenonum, Calcarea Carbonica, Graphites, Lycopodium Clavatum, Anacardium Orientale, Colchicum Autumnale, Nux Vomica, Phytolacca Decandra, Pulsatilla (Pratensis), Histaminum Hydrochloricum

Active Ingredient(s):
  • 6 [hp_X]/mL APIS MELLIFERA;
  • 6 [hp_X]/mL CAPSICUM;
  • 6 [hp_X]/mL CHASTE TREE FRUIT;
  • 6 [hp_X]/mL CHELIDONIUM MAJUS WHOLE;
  • 30 [hp_C]/mL COLCHICUM AUTUMNALE BULB;
  • 12 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE;
  • 6 [hp_X]/mL FUCUS VESICULOSUS;
  • 3 [hp_X]/mL GALIUM APARINE WHOLE;
  • 12 [hp_X]/mL GRAPHITE;
  • 200 [hp_C]/mL HISTAMINE DIHYDROCHLORIDE;
  • 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 30 [hp_C]/mL PHYTOLACCA AMERICANA ROOT;
  • 30 [hp_C]/mL PULSATILLA PRATENSIS WHOLE;
  • 30 [hp_C]/mL SEMECARPUS ANACARDIUM JUICE;
  • 12 [hp_X]/mL SMILAX ORNATA ROOT;
  • 12 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE;
  • 30 [hp_C]/mL STRYCHNOS NUX-VOMICA SEED;
  • 6 [hp_X]/mL TARAXACUM OFFICINALE;
  • 12 [hp_X]/mL UBIDECARENONE;
  • 6 [hp_X]/mL URTICA DIOICA WHOLE;
  • 6 [hp_X]/mL ZANTHOXYLUM AMERICANUM BARK


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Bee Venoms [CS];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [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];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS];
  • Standardized Insect Venom Allergenic Extract [EPC];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Heilen
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/21/2022

Package Information

No. Package Code Package Description Billing Unit
170719-0003-130 mL in 1 BOTTLE, DROPPER (70719-0003-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70719-0003The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEHeilenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGalium Aparine, Agnus Castus, Apis Mellifica, Capsicum Annuum, Chelidonium Majus, Taraxacum Officinale, Urtica Dioica, Xanthoxylum Fraxineum, Fucus Vesiculosus, Kali Phosphoricum, Magnesia Phosphorica, Natrum Phosphoricum, Sarsaparilla (smilax Regelii), Ubidecarenonum, Calcarea Carbonica, Graphites, Lycopodium Clavatum, Anacardium Orientale, Colchicum Autumnale, Nux Vomica, Phytolacca Decandra, Pulsatilla (Pratensis), Histaminum HydrochloricumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/21/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEHeilenName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAPIS MELLIFERA; CAPSICUM; CHASTE TREE FRUIT; CHELIDONIUM MAJUS WHOLE; COLCHICUM AUTUMNALE BULB; DIBASIC POTASSIUM PHOSPHATE; FUCUS VESICULOSUS; GALIUM APARINE WHOLE; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; PULSATILLA PRATENSIS WHOLE; SEMECARPUS ANACARDIUM JUICE; SMILAX ORNATA ROOT; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRYCHNOS NUX-VOMICA SEED; TARAXACUM OFFICINALE; UBIDECARENONE; URTICA DIOICA WHOLE; ZANTHOXYLUM AMERICANUM BARKAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6; 6; 6; 6; 30; 12; 6; 3; 12; 200; 12; 12; 12; 30; 30; 30; 12; 12; 30; 6; 12; 6; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [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], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vegetable Proteins [CS] 

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This page was last updated on: 2/1/2023