NDC 52731-7005 Respiratory Complex

Antimonium Tartaricum, Bryonia, Chelidonium Majus, Echinacea Angustifolia, Hepar Sulphuris Calcareum, Hepatica Tribola, Lycopodium Clavatum, Phosphorus, Stannum Metallicum, Sticta Pulmonaria

NDC Product Code 52731-7005

NDC Code: 52731-7005

Proprietary Name: Respiratory Complex What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Antimonium Tartaricum, Bryonia, Chelidonium Majus, Echinacea Angustifolia, Hepar Sulphuris Calcareum, Hepatica Tribola, Lycopodium Clavatum, Phosphorus, Stannum Metallicum, Sticta Pulmonaria What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 52731 - Nova Homeopathic Therapeutics, Inc.
    • 52731-7005 - Respiratory Complex

NDC 52731-7005-2

Package Description: 1 BOTTLE in 1 BOX > 50 mL in 1 BOTTLE (52731-7005-1)

NDC Product Information

Respiratory Complex with NDC 52731-7005 is a a human over the counter drug product labeled by Nova Homeopathic Therapeutics, Inc.. The generic name of Respiratory Complex is antimonium tartaricum, bryonia, chelidonium majus, echinacea angustifolia, hepar sulphuris calcareum, hepatica tribola, lycopodium clavatum, phosphorus, stannum metallicum, sticta pulmonaria. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Nova Homeopathic Therapeutics, 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.

Respiratory Complex 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.

  • ANTIMONY POTASSIUM TARTRATE 6 [hp_X]/mL
  • BRYONIA ALBA ROOT 4 [hp_X]/mL
  • CHELIDONIUM MAJUS 6 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 4 [hp_X]/mL
  • CALCIUM SULFIDE 8 [hp_X]/mL
  • HEPATICA NOBILIS VAR. OBTUSA 4 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • TIN 8 [hp_X]/mL
  • LOBARIA PULMONARIA 4 [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)

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: Nova Homeopathic Therapeutics, Inc.
Labeler Code: 52731
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: 06-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2017 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: E 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’.

* Please review the disclaimer below.

Respiratory Complex 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

Purpose:

Suggested use for one or more of the following symptoms:Cough,asthma,lung congestion, and bronchial infections.

Usage And Dosage:

For oral use only.

Dosage & Administration

Adults:    In Acute Phase:            12-15 drops, every half hour until relief occurs    When Relief Occurs:            12-15 drops, 4-6 times per dayChildren 2-12 years:            8-10 drops, 4-6 times per day

Warnings:

Keep out of reach of children.

Warnings

If symptoms persist, consult a physician.Do not use if ring on bottom of cap is broken or missing.

Active Ingredients:

Antimonium tartaricum 6X, Bryonia 4X, Chelidonium majus 6X, Echinacea angustifolia 4X, Hepar sulphuris calcareum 8X, Hepatica tribola 4X, Lycopodium clavatum 6X, Phosphorus 12X, Stannum metallicum 8X, Sticta pulmonaria 4X

Inactive Ingredients:

Alcohol, 20% USP

Otc - Questions

Manufactured by Nova Homeopathic Therapeutics Inc., Albuquerque, New Mexico USA 871091-800-225-8094

* Please review the disclaimer below.

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