FDA.reportPublic FDA data

Lung Distress

Manufacturer
Liddell Laboratories | Apotheca Company
Effective date
2021-11-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:28:52

Label at a glance#

ProductLung Distress
Active ingredientARSENIC TRIIODIDE, BLATTA ORIENTALIS, BRYONIA ALBA ROOT, ACTIVATED CHARCOAL, EUPATORIUM PERFOLIATUM FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, IPECAC, SUS SCROFA LUNG, SODIUM SULFATE, NITRIC ACID, ASPIDOSPERMA QUEBRACHO-BLANCO BARK, EUROPEAN ELDERBERRY, LOBARIA PULMONARIA, URTICA URENS
Label structure9 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 severe symptoms, dosage may be taken up to six times the first day. Children 12 and under: Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Arsenicum Iodatum 200C, Blatta Orientalis 30C, Bryonia 6X, Carbo Vegetabilis 12X, Eupatorium Perfoliatum 6X, Histaminum Hydrochloricum 200C, Ipecacuanha 4X, Lung Suis 6X, Natrum Sulphuricum 30C, Nitricum Acidum 200C, Quebracho 3X, Sambucus Nigra 3X, Sticta Pulmonaria 200C, Urtica Urens 6X, 200C.

USES:

OTC - PURPOSE SECTION

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.

WARNINGS:

WARNINGS SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

If pregnant or breast-feeding, ask a doctor before using product.

OTHER INFORMATION: Store at room temperature.

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12: Spray twice under the tongue 3 times per day. For severe symptoms, dosage may be taken up to six times the first day.

Children 12 and under: Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

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.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY:

LIDDELL LABORATORIES

201 APPLE BLVD.

WOODBINE, IA 51579

WWW.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL
LABORATORIES

EST 1994


16 Lu
Lung Distress


May relieve minor symptoms

associated with breathing

difficulties: congestion, coughing,

wheezing, tight feeling in the chest.


HOMEOPATHIC


DOCTOR FORMULATED

Readily absorbed. Safe.
No known side effects. Easy to use.


1.0 FL OZ. (30 ml)

Lung Distress lblLung Distress lbl

Lung Distress ctnLung Distress ctn

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0242-12021-11-08C16284748780-19d75b9d0-bbb7-f424-e053-dadaa90a57ceDrug Facts:
50845-0242-12020-01-31C16284748780-19d75b9d0-bbb7-f424-e053-dadaa90a57ceDrug Facts:

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-024250845-0242-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARSENIC TRIIODIDE3029988O2TACTIB
BLATTA ORIENTALIS535787266DACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
ACTIVATED CHARCOAL2P3VWU3H10ACTIB
EUPATORIUM PERFOLIATUM FLOWERING TOP1W0775VX6EACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
IPECAC62I3C8233LACTIB
SUS SCROFA LUNG7GL3G1COB3ACTIB
SODIUM SULFATE0YPR65R21JACTIB
NITRIC ACID411VRN1TV4ACTIB
ASPIDOSPERMA QUEBRACHO-BLANCO BARK52B1340190ACTIB
EUROPEAN ELDERBERRYBQY1UBX046ACTIB
LOBARIA PULMONARIAD1YM0P5Z2TACTIB
URTICA URENSIHN2NQ5OF9ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML · Source PDF

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6ca1d01d-5a3a-45c5-955c-7b742ba3fb065be03aca-b66e-461b-ab3e-d34db136446c2021-11-08WarningsExact identifier
spl id: 6ca1d01d-5a3a-45c5-955c-7b742ba3fb06
spl set id: 5be03aca-b66e-461b-ab3e-d34db136446c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.