Bronchi

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2022-03-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:05:41

Label at a glance#

ProductBronchi HP
Active ingredientACTIVATED CHARCOAL, COPPER, DROSERA ROTUNDIFOLIA, CALCIUM SULFIDE, IPECAC, LACHESIS MUTA VENOM, LOBELIA INFLATA WHOLE, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED
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 7 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): 9.09% of Carbo Vegetabilis 30X, Cuprum Metallicum 30X, Drosera (Rotundifolia) 30X, Hepar Sulphuris Calcareum 30X, Ipecacuanha 30X, Lachesis Mutus 30X, Lobelia Inflata 30X, Phosphorus 30X, Pulsatilla (Pratensis) 30X, Rumex Crispus 30X, Spongia Tosta 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms of chronic cough, heaviness in chest, and bronchial irritation.**

**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 7 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 symptoms of chronic cough, heaviness in chest, and bronchial irritation.**

**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

BRONCHI HP

1 fl. oz. (30 ml)

Bronchi HPBronchi HP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0549-12022-03-18C16284748780-1d6a99b39-e06c-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0549-12022-01-28C16284748780-1d6a99b39-e06c-a426-e053-dadaa90af4c2DRUG FACTS:

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-054944911-0549-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
4027731b-056d-47d5-9632-a1035c0b89cf64565ea2-3e9b-4e39-89b8-2477d66fbf462022-03-18WarningsExact identifier
spl id: 4027731b-056d-47d5-9632-a1035c0b89cf
spl set id: 64565ea2-3e9b-4e39-89b8-2477d66fbf46

Reported adverse events (FAERS/openFDA)#

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