Pneumopar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-03-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:05:10

Label at a glance#

ProductPneumopar
Active ingredientLOBELIA INFLATA, SUS SCROFA LUNG, COMFREY ROOT, ARSENIC TRIOXIDE, BLATTA ORIENTALIS, BRYONIA ALBA ROOT, PHOSPHORUS, SILICON DIOXIDE, SULFUR
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 3 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) 12.49% of Arsenicum Album 12X, Blatta Orientalis 12X, Bryonia (Alba) 12X, Lung (Suis) 6X, Phosphorus 12X, Silicea 12, Sulphur 12X, Symphytum Officinale 6X; 0.10% of Lobelia Inflata 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve wheezing, shortness of breath, constrictive feeling in the chest and cough.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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 3 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 wheezing, shortness of breath, constrictive feeling in the chest and cough.**

**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
PNEUMOPAR
1 fl. oz. (30 ml)

PneumoparPneumopar

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0374-12022-03-23C16284748780-1d6a99b39-3922-a426-e053-dadaa90af4c2Drug Facts:
44911-0374-12022-01-28C16284748780-1d6a99b39-3922-a426-e053-dadaa90af4c2Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-037444911-0374-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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
b0282e4a-7670-4a1a-a687-938a1f8baf9d7401ab08-29c2-4c80-8d9f-dc987b688fb32022-03-23WarningsExact identifier
spl id: b0282e4a-7670-4a1a-a687-938a1f8baf9d
spl set id: 7401ab08-29c2-4c80-8d9f-dc987b688fb3

Reported adverse events (FAERS/openFDA)#

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