50845-0275 NDC - LUNG DISTRESS (BLATTA ORIENTALIS, BRYONIA (ALBA), CARBO VEGETABILIS, EUPATORIUM PERFOLIATUM, HISTAMINUM HYDROCHLORICUM, IODIUM, IPECACUANHA, LUNG SUIS, NATRUM SULPHURICUM, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), QUEBRACHO, SAMBUCUS NIGRA, STICTA PULMONARIA, URTICA URENS)

Drug Information

  • Product NDC: 50845-0275
  • Proprietary Name: Lung Distress
  • Non Proprietary Name: Blatta Orientalis, Bryonia (Alba), Carbo Vegetabilis, Eupatorium Perfoliatum, Histaminum Hydrochloricum, Iodium, Ipecacuanha, Lung Suis, Natrum Sulphuricum, Nitricum Acidum, Pulsatilla (Pratensis), Quebracho, Sambucus Nigra, Sticta Pulmonaria, Urtica Urens
  • Active Ingredient(s): 12 [hp_X]/mL ACTIVATED CHARCOAL; 12 [hp_X]/mL ASPIDOSPERMA QUEBRACHO-BLANCO BARK; 30 [hp_C]/mL BLATTA ORIENTALIS; 6 [hp_X]/mL BRYONIA ALBA ROOT; 6 [hp_X]/mL EUPATORIUM PERFOLIATUM FLOWERING TOP; 200 [hp_C]/mL HISTAMINE DIHYDROCHLORIDE; 200 [hp_C]/mL IODINE; 4 [hp_X]/mL IPECAC; 200 [hp_C]/mL LOBARIA PULMONARIA; 200 [hp_C]/mL NITRIC ACID; 30 [hp_C]/mL PULSATILLA PRATENSIS WHOLE; 3 [hp_X]/mL SAMBUCUS NIGRA FLOWERING TOP; 30 [hp_C]/mL SODIUM SULFATE; 6 [hp_X]/mL SUS SCROFA LUNG; 6 [hp_X]/mL URTICA URENS WHOLE
  • Administration Route(s): ORAL
  • Dosage Form(s): SPRAY
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Insect Proteins [CS]; Non-Standardized Insect Allergenic Extract [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Liddell Laboratories
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/5/2021

Package Information

No. Package Code Package Description Billing Unit
150845-0275-21 BOTTLE, SPRAY in 1 CARTON (50845-0275-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0275-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50845-0275The 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 NAMELung DistressThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEBlatta Orientalis, Bryonia (Alba), Carbo Vegetabilis, Eupatorium Perfoliatum, Histaminum Hydrochloricum, Iodium, Ipecacuanha, Lung Suis, Natrum Sulphuricum, Nitricum Acidum, Pulsatilla (Pratensis), Quebracho, Sambucus Nigra, Sticta Pulmonaria, Urtica UrensThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe 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 DATE10/5/2021This 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 LaboratoriesName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; ASPIDOSPERMA QUEBRACHO-BLANCO BARK; BLATTA ORIENTALIS; BRYONIA ALBA ROOT; EUPATORIUM PERFOLIATUM FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; IODINE; IPECAC; LOBARIA PULMONARIA; NITRIC ACID; PULSATILLA PRATENSIS WHOLE; SAMBUCUS NIGRA FLOWERING TOP; SODIUM SULFATE; SUS SCROFA LUNG; URTICA URENS WHOLEAn 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 STRENGTH12; 12; 30; 6; 6; 200; 200; 4; 200; 200; 30; 3; 30; 6; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/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; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC] 

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This page was last updated on: 12/6/2025

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