Home DailyMed 776844d7-afcd-4891-8684-2511678c5475 Lung Distress Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Liddell Laboratories | Apotheca Company
Effective date 2024-11-04
Label type HUMAN OTC DRUG LABEL
Version 2
Source full-release
Hydrated at 2026-06-01 02:28:46 Label at a glance# Product Lung Distress
Active ingredient BLATTA ORIENTALIS, BRYONIA ALBA ROOT, ACTIVATED CHARCOAL, EUPATORIUM PERFOLIATUM FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, IODINE, IPECAC, SUS SCROFA LUNG, SODIUM SULFATE, NITRIC ACID, PULSATILLA PRATENSIS WHOLE, ASPIDOSPERMA QUEBRACHO-BLANCO BARK, SAMBUCUS NIGRA FLOWERING TOP, LOBARIA PULMONARIA, URTICA URENS WHOLE
Label structure 9 sections
Indications and uses May temporarily relieve minor symptoms associated with breathing difficulties: • congestion • coughing • wheezing • tight feeling in the chest** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Dosage and administration Adults and children over 12: Spray twice under the tongue 3 times per day. For frequent symptoms, dosage may be taken up to six times the first day. Children 12 and under: Consult a doctor prior to use.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 50845-0275-1 Lung Distress 30 mL in 1 BOTTLE, SPRAY SPRAY 30 2 50845-0275-2 Lung Distress 1 in 1 CARTON SPRAY 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 50845-0275 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) SPRAY [LIDDELL LABORATORIES] 2 Current NDC, Legacy NDC, 2 package rows 20241105_776844d7-afcd-4891-8684-2511678c5475.zip
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 22 matching rows.
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 BLATTA ORIENTALIS BRYONIA ALBA ROOT ACTIVATED CHARCOAL EUPATORIUM PERFOLIATUM FLOWERING TOP HISTAMINE DIHYDROCHLORIDE HISTAMINE IODINE IPECAC SUS SCROFA LUNG SODIUM SULFATE SODIUM SULFATE ANHYDROUS NITRIC ACID PULSATILLA PRATENSIS WHOLE ASPIDOSPERMA QUEBRACHO-BLANCO BARK SAMBUCUS NIGRA FLOWERING TOP LOBARIA PULMONARIA URTICA URENS WHOLE URTICA URENS WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 17 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join 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 Liddell Laboratories 776844d7-afcd-4891-8684-2511678c5475 2024-11-04 Warnings Exact identifier ndc (package): 50845-0275-2 ndc (package): 50845-0275-1 ndc (product): 50845-0275 ndc11 (package): 50845027501 ndc11 (package): 50845027502 spl id: 3d615630-f936-4962-af1d-0525c3cae9c4 spl set id: 776844d7-afcd-4891-8684-2511678c5475
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.