NDC 44911-0007 Bronchi HP

Carbo Vegetabilis, Cuprum Metallicum, Drosera, Hepar Sulphuris Calcareum, Ipecacuanha, Lachesis Mutus, Lobelia Inflata, Phosphorus, Pulsatilla, Rumex Crispus, Spongia Tosta,

NDC Product Information

Bronchi HP with NDC 44911-0007 is a a human over the counter drug product labeled by Energique, Inc.. The generic name of Bronchi HP is carbo vegetabilis, cuprum metallicum, drosera, hepar sulphuris calcareum, ipecacuanha, lachesis mutus, lobelia inflata, phosphorus, pulsatilla, rumex crispus, spongia tosta, . The product's dosage form is liquid and is administered via oral form.

Labeler Name: Energique, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Bronchi HP Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • COPPER 30 [hp_X]/mL
  • DROSERA ANGLICA 30 [hp_X]/mL
  • CALCIUM SULFIDE 30 [hp_X]/mL
  • IPECAC 30 [hp_X]/mL
  • LOBELIA INFLATA 30 [hp_X]/mL
  • PHOSPHORUS 30 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ALCOHOL (UNII: 3K9958V90M)
  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Energique, Inc.
Labeler Code: 44911
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-23-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 05-15-2023 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Bronchi HP Product Label Images

Bronchi HP Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Carbo Vegetabilis 30X, Cuprum Metallicum 30X, Drosera 30X, Hepar Sulphuris Calcareum 30X, Ipecacuanha 30X, Lachesis Mutus 30X, Lobelia Inflata 30X, Phosphorus 30X, Pulsatilla (Vulgaris) 30X, Rumex Crispus 30X, Spongia Tosta 30X.


May temporarily relieve symptoms of chronic cough, heaviness in the chest, and bronchial irritation.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

May temporarily relieve symptoms of chronic cough, heaviness in the chest, and bronchial irritation.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.


If pregnant or breast-feeding, ask a health care 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:

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


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

Inactive Ingredients:

Demineralized water, 20% Ethanol.


Dist. by Energique, Inc.201 Apple BlvdWoodbine, IA 51579  800.869.8078

Package Label Display:


* Please review the disclaimer below.