Bronchi HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:35:11

Label at a glance#

ProductBronchi HP
Active ingredientACTIVATED CHARCOAL, COPPER, DROSERA ROTUNDIFOLIA, IPECAC, LACHESIS MUTA VENOM, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTED
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Carbo Vegetabilis 30X, Cuprum Metallicum 30X, Drosera Rotundifolia 30X, Ipecacuanha 30X, Lachesis Mutus 30X, Lobelia Inflata 30X, Phosphorus 30X, Rumex Crispus 30X, Spongia Tosta 30X

INDICATIONS & USAGE SECTION

USES: Temporarily relieves dry, spasmodic, irritating cough with hoarseness.**

WARNINGS SECTION

WARNING:

  • Consult a physician for use in children under 12 years of age.
  • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
  • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. 
  • If cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash, or persistent headache, consult a doctor.
  • Do not use if TAMPER EVIDENT seal is broken or missing.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults and children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

REFERENCES SECTION

*The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

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

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS?
Natural Creations / Woodbine, IA / 51579 712-647-1600

OTC - PURPOSE SECTION

USES: Temporarily relieves dry, spasmodic, irritating cough with hoarseness.**

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0010-1

BRONCHI HP

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

UPC: 877730000460

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730000460GTIN-13: 0877730000460
EAN-13: 0877730000460
GTIN-12: 877730000460
UPC-A: 877730000460
GTIN storage (14 digits): 00877730000460
BRONCHI HP.jpg

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
43406-0010-12022-03-03C16284748780-19855d018-dfd9-cd31-e053-dbdaa90ab51aBRONCHI HP
43406-0010-12022-01-28C16284748780-19855d018-dfd9-cd31-e053-dbdaa90ab51aBRONCHI HP
43406-0010-12020-09-11C16284748780-19855d018-dfd9-cd31-e053-dbdaa90ab51aBRONCHI HP
43406-0010-12019-11-27C16284748780-19855d018-dfd9-cd31-e053-dbdaa90ab51aBRONCHI HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0010-1Bronchi HP30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACTIVATED CHARCOALACTIVE INGREDIENT2P3VWU3H101
COPPERACTIVE INGREDIENT789U1901C51
DROSERA ROTUNDIFOLIAACTIVE INGREDIENTQR44N9XPJQ1
IPECACACTIVE INGREDIENT62I3C8233L1
LACHESIS MUTA VENOMACTIVE INGREDIENTVSW71SS07I1
LOBELIA INFLATAACTIVE INGREDIENT9PP1T3TC5U1
PHOSPHORUSACTIVE INGREDIENT27YLU75U4W1
PULSATILLA VULGARISACTIVE INGREDIENTI76KB35JEV1
RUMEX CRISPUS ROOTACTIVE INGREDIENT9N1RM2S62C1
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE INGREDIENT1PIP394IID1
ACTIVATED CHARCOALACTIVE MOIETY2P3VWU3H101
COPPERACTIVE MOIETY789U1901C51
DROSERA ROTUNDIFOLIAACTIVE MOIETYQR44N9XPJQ1
IPECACACTIVE MOIETY62I3C8233L1
LACHESIS MUTA VENOMACTIVE MOIETYVSW71SS07I1
LOBELIA INFLATAACTIVE MOIETY9PP1T3TC5U1
PHOSPHORUSACTIVE MOIETY27YLU75U4W1
PULSATILLA VULGARISACTIVE MOIETYI76KB35JEV1
RUMEX CRISPUS ROOTACTIVE MOIETY9N1RM2S62C1
SPONGIA OFFICINALIS SKELETON, ROASTEDACTIVE MOIETY1PIP394IID1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
43406-001043406-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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
Bronchi HPACTIVATED CHARCOAL, COPPER, DROSERA ROTUNDIFOLIA, IPECAC, LACHESIS MUTA VENOM, LOBELIA INFLATA, PHOSPHORUS, PULSATILLA VULGARIS, RUMEX CRISPUS ROOT, SPONGIA OFFICINALIS SKELETON, ROASTEDNatural Creations, Inc.5f5c2c8f-1c6d-4def-b202-bd0e596230a02025-11-13WarningsExact identifier
ndc (package): 43406-0010-1
ndc (product): 43406-0010
ndc11 (package): 43406001001
spl id: 6ab2b46b-df3f-4897-be74-fe6a9ec68382
spl set id: 5f5c2c8f-1c6d-4def-b202-bd0e596230a0

Reported adverse events (FAERS/openFDA)#

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