50845-0034 NDC - NICOTINE FREE (ABIES NIGRA, ACONITUM NAPELLUS, ARSENICUM IODATUM, AVENA SATIVA, IGNATIA AMARA, LUNG SUIS, NUX VOMICA, PLANTAGO MAJOR, QUEBRACHO, STICTA PULMONARIA, TABACUM,)

Drug Information

Product NDC: 50845-0034

Proprietary Name: Nicotine Free

Non Proprietary Name: Abies Nigra, Aconitum Napellus, Arsenicum Iodatum, Avena Sativa, Ignatia Amara, Lung Suis, Nux Vomica, Plantago Major, Quebracho, Sticta Pulmonaria, Tabacum,

Active Ingredient(s):
  • 200 [hp_C]/mL ACONITUM NAPELLUS;
  • 200 [hp_C]/mL ARSENIC TRIIODIDE;
  • 3 [hp_X]/mL ASPIDOSPERMA QUEBRACHO-BLANCO BARK;
  • 1 [hp_X]/mL AVENA SATIVA FLOWERING TOP;
  • 200 [hp_C]/mL LOBARIA PULMONARIA;
  • 10 [hp_X]/mL PICEA MARIANA RESIN;
  • 3 [hp_X]/mL PLANTAGO MAJOR;
  • 200 [hp_C]/mL STRYCHNOS IGNATII SEED;
  • 10 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED;
  • 6 [hp_X]/mL SUS SCROFA LUNG;
  • 200 [hp_C]/mL TOBACCO LEAF


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased IgG Production [PE];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS]

Labeler Information

Labeler Name: Liddell Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/10/2014

Package Information

No. Package Code Package Description Billing Unit
150845-0034-130 mL in 1 BOTTLE, SPRAY (50845-0034-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50845-0034The 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 NAMENicotine FreeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAbies Nigra, Aconitum Napellus, Arsenicum Iodatum, Avena Sativa, Ignatia Amara, Lung Suis, Nux Vomica, Plantago Major, Quebracho, Sticta Pulmonaria, Tabacum,The 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 DATE1/10/2014This 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 NAMELiddell Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS; ARSENIC TRIIODIDE; ASPIDOSPERMA QUEBRACHO-BLANCO BARK; AVENA SATIVA FLOWERING TOP; LOBARIA PULMONARIA; PICEA MARIANA RESIN; PLANTAGO MAJOR; STRYCHNOS IGNATII SEED; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA LUNG; TOBACCO LEAFAn 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 STRENGTH200; 200; 3; 1; 200; 10; 3; 200; 10; 6; 200 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS] 

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