Lungex

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-28
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:28:32

Label at a glance#

ProductLungex II
Active ingredientGINKGO, SUS SCROFA COLON, SUS SCROFA LUNG, SUS SCROFA PANCREAS, GERMANIUM SESQUIOXIDE, COPPER, MANGANESE, TIN, OXOGLURIC ACID, CITRIC ACID MONOHYDRATE, FUMARIC ACID, MALIC ACID, PYRUVIC ACID, SUCCINIC ACID, 1,2-NAPHTHOQUINONE, ARSENIC, OYSTER SHELL CALCIUM CARBONATE, CRUDE, ACONITIC ACID, SODIUM DIETHYL OXALACETATE, PHOSPHORUS
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 33.30% Of Natrum Oxalaceticum 12X, 30X. 1.11% Of Alpha-Ketoglutaricum Acidum+ 8X, 12X, 30X; Citricum Acidum 8X, 12X, 30X, Pyruvic Acid 8X, 12X, 30X; Arsenicum Metallicum 12X, Calcarea Carbonica 12X, Cuprum Metallicum 12X, Manganum Metallicum 12X, Stannum Metallicum 12X; Colon (Suis) 12X, 30X, Fumaricum Acidum 12X, 30X, Lung (Suis) 12X, 30X, Malicum Acidum 12X, 30X, Pancreas Suis 12X, 30X, Phosphorus 12X, 30X, Succinicum Acidum 12X, 30X; Aconiticum Acidum, Cis- 30X, Naphthochinonum 30X, 0.01% Of Colon (Suis) 6X, Ginkgo Biloba 6X, Lung (Suis) 6X, Pancreas Suis 6X; Cuprum Metallicum 8X, Fumaricum Acidum 8X, Germanium Sesquioxide 8X, Malicum Acidum 8X, Manganum Metallicum 8X, Stannum Metallicum 8X, Succinicum Acidum 8X; Naphthochinonum 9X, 12X; Aconiticum Acidum, Cis- 12X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve coughing, wheezing, diarrhea, abdominal pain, and bloating.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

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

Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

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 contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 2 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve coughing, wheezing, diarrhea, abdominal pain, and bloating.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579   800-869-8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

LUNGEX II

1 fl. oz. (30 ml)

Lungex IILungex II

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0439-12024-10-28C16284748780-1ba0f9c33-4d39-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0439-12024-01-30C16284748780-1ba0f9c33-4d39-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0439-12021-04-12C16284748780-1ba0f9c33-4d39-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0439-12021-01-29C16284748780-1ba0f9c33-4d39-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0439-1LungexII30 mL in 1 BOTTLE, DROPPERLIQUID305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0439LUNGEX II (GINKGO BILOBA, COLON (SUIS), LUNG (SUIS), PANCREAS SUIS, GERMANIUM SESQUIOXIDE, CUPRUM METALLICUM, MANGANUM METALLICUM, STANNUM METALLICUM, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALIC ACID, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOQUINONE, ARSENICUM METALLICUM, CALCAREA CARBONICA, ACONITICUM ACIDUM, CIS, NATRUM OXALACETICUM, PHOSPHORUS) LIQUID [ENERGIQUE, INC.]5Current NDC, Legacy NDC, 1 package rows20241030_ddf7fc46-95b7-44b4-b7ca-96a066a3fa2b.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-043944911-0439-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
Lungex IIGINKGO BILOBA, COLON (SUIS), LUNG (SUIS), PANCREAS SUIS, GERMANIUM SESQUIOXIDE, CUPRUM METALLICUM, MANGANUM METALLICUM, STANNUM METALLICUM, ALPHA-KETOGLUTARICUM ACIDUM, CITRICUM ACIDUM, FUMARICUM ACIDUM, MALIC ACID, PYRUVIC ACID, SUCCINICUM ACIDUM, NAPHTHOQUINONE, ARSENICUM METALLICUM, CALCAREA CARBONICA, ACONITICUM ACIDUM, CIS, NATRUM OXALACETICUM, PHOSPHORUSEnergique, Inc.ddf7fc46-95b7-44b4-b7ca-96a066a3fa2b2024-10-28WarningsExact identifier
ndc (package): 44911-0439-1
ndc (product): 44911-0439
ndc11 (package): 44911043901
spl id: 6b5ca9cb-ad13-44ab-a49f-4d569a01f6a7
spl set id: ddf7fc46-95b7-44b4-b7ca-96a066a3fa2b

Reported adverse events (FAERS/openFDA)#

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