NDC 52731-7031 Fever Complex
Aconitum Napellus, Arnica Montana, Baptisia Tinctoria, Berberis Vulgaris, Cactus Grandiflorus,chelidonium Majus, Echinacea Angustifolia, Ferrum Phosphoricum, Hepar Sulfuris Calcareum, Urtica Urens
NDC Product Code 52731-7031
Proprietary Name: Fever 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: Aconitum Napellus, Arnica Montana, Baptisia Tinctoria, Berberis Vulgaris, Cactus Grandiflorus,chelidonium Majus, Echinacea Angustifolia, Ferrum Phosphoricum, Hepar Sulfuris Calcareum, Urtica Urens 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.
Code Structure
- 52731 - Nova Homeopathic Therapeutics, Inc.
- 52731-7031 - Fever Complex
NDC 52731-7031-2
Package Description: 1 BOTTLE in 1 BOX > 50 mL in 1 BOTTLE (52731-7031-1)
NDC Product Information
Fever Complex with NDC 52731-7031 is a a human over the counter drug product labeled by Nova Homeopathic Therapeutics, Inc.. The generic name of Fever Complex is aconitum napellus, arnica montana, baptisia tinctoria, berberis vulgaris, cactus grandiflorus,chelidonium majus, echinacea angustifolia, ferrum phosphoricum, hepar sulfuris calcareum, urtica urens. 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.
Fever 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.
- ACONITUM NAPELLUS 6 [hp_X]/mL
- ARNICA MONTANA 6 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 4 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 4 [hp_X]/mL
- SELENICEREUS GRANDIFLORUS STEM 6 [hp_X]/mL
- CHELIDONIUM MAJUS 6 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 2 [hp_X]/mL
- FERRUM PHOSPHORICUM 8 [hp_X]/mL
- CALCIUM SULFIDE 8 [hp_X]/mL
- URTICA URENS 2 [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 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.
Fever Complex Product Label Images
Fever 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:
- Usage And Dosage:
- Dosage & Administration
- Warnings:
- Warnings
- Active Ingredients:
- Inactive Ingredients:
- Otc - Questions
Purpose:
Suggested use for one or more of the following symptoms:Intermittent fever, dry heat of skin, mucous draining and inflammatory fever.
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 dayInfants 0-24 months: 4 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:
Aconitum napellus 6X, Arnica montana 6X, Baptisia tinctoria 4X, Berberis vulgaris 4X, Cactus grandiflorus 6X,Chelidonium majus 6X, Echinacea angustifolia 2X, Ferrum phosphoricum 8X, Hepar sulfuris calcareum 8X, Urtica urens 2X
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.