Lung Detox

Manufacturer
ProBLEN
Effective date
2022-11-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:18:39

Label at a glance#

ProductLung Detox
Active ingredientSILVER NITRATE, ARSENIC TRIOXIDE, MILK THISTLE, PORK LIVER, MERCURIC CHLORIDE, LEAD
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Argentum nitricum 200C, Arsenicum album 200C, Carduus marianus 1X, Hepar suis 6X, Mercurius corrosivus 200C,

Plumbum metallicum 200C.

*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INDICATIONS & USAGE SECTION

Indications: Detoxifies the lungs from inhaled indoor and outdoor pollutants and relieves associated symptoms: shortness of breath, wheezing, coughing, lack of energy. Homeopathic. Doctor formulated. Readily absorbed, safe, no known side effects, easy to use.*

WARNINGS SECTION

Warnings: 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If pregnant or breast feeding, ask a doctor before using product.

DOSAGE & ADMINISTRATION SECTION

Directions: Adults & children over 12: Spray twice under the tongue three times per day. Children 2 to 12: Spray once under the tongue three times per day. Children under 2: Consult a doctor prior to use.

OTHER SAFETY INFORMATION

Other information: Store at room temperature.

Tamper Evident: The bottle has a seal imprinted with the words "Sealed for your Safety". Do not use if this seal is missing or broken.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic alcohol 20% v/v, USP Purified water.

OTC - QUESTIONS SECTION

Distributed By: ProBLEN (888) 326 - 2121

www.problen.com 3021 Ridge Rd., Rockwall, TX 75032

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43853-0042-1

Lung Detox

HOMEOPATHY

ORGANOTHERAPY

1.0 FL OZ. (30mL) 20% ALCOHOL

1 fl. oz. bottle label1 fl. oz. bottle label

OTC - PURPOSE SECTION

Purposes: Symptom relief of airborne pollution

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43853-0042-1Lung Detox30 mL in 1 BOTTLELIQUID303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43853-0042LUNG DETOX (ARGENTUM NITRICUM, ARSENICUM ALBUM, CARDUUS MARIANUS, HEPAR SUIS, MERCURIUS CORROSIVUS, PLUMBUM METALLICUM) LIQUID [PROBLEN]3Current NDC, Legacy NDC, 1 package rows20221201_c4be510c-2aac-4737-ba05-eccac3aed941.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43853-004243853-0042-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

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
Lung DetoxARGENTUM NITRICUM, ARSENICUM ALBUM, CARDUUS MARIANUS, HEPAR SUIS, MERCURIUS CORROSIVUS, PLUMBUM METALLICUMProBLENc4be510c-2aac-4737-ba05-eccac3aed9412022-11-30WarningsExact identifier
ndc (package): 43853-0042-1
ndc (product): 43853-0042
ndc11 (package): 43853004201
spl id: eeb45ede-aec6-2289-e053-2995a90af21a
spl set id: c4be510c-2aac-4737-ba05-eccac3aed941

Reported adverse events (FAERS/openFDA)#

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