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  4. NDC Product Code: 66492-001 Flu Terminator Drops

NDC 66492-001 Flu Terminator Drops

Gelsemium,Zincum Gluconicum,Zincum Metallicum,Aconitum Napellus,Eupatorium - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66492-001?
  4. Flu Terminator Drops Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
66492-001
Proprietary Name:
Flu Terminator Drops
Non-Proprietary Name: [1]
Gelsemium, Zincum Gluconicum, Zincum Metallicum, Aconitum Napellus, Eupatorium Perfoliatum, Sulphur, Phosphorus, Asclepias Vincetoxicum, Influenzinum, Anas Barbariae.
Substance Name: [2]
Aconitum Napellus; Cairina Moschata Heart/liver Autolysate; Cynanchum Vincetoxicum Root; Eupatorium Perfoliatum Flowering Top; Gelsemium Sempervirens Root; Influenza A Virus; Influenza B Virus; Phosphorus; Sulfur; Zinc; Zinc Gluconate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Be Well Medical Dba Richard Clement Nutrition Y Be Well Homeopathics
    Labeler Code:
    66492
    Product Label ID:
    c818b723-e038-47b0-940a-f2bb7edfd69c
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-01-2000
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 66492-001-02

    Package Description: 58.5 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 66492-001?

    The NDC code 66492-001 is assigned by the FDA to the product Flu Terminator Drops which is a human over the counter drug product labeled by Be Well Medical Dba Richard Clement Nutrition Y Be Well Homeopathics. The generic name of Flu Terminator Drops is gelsemium, zincum gluconicum, zincum metallicum, aconitum napellus, eupatorium perfoliatum, sulphur, phosphorus, asclepias vincetoxicum, influenzinum, anas barbariae.. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 66492-001-02 58.5 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for Flu Terminator Drops?

    USES: Temporarily relieves flu, fever and associated viral conditions.

    What are Flu Terminator Drops Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • ACONITUM NAPELLUS 4 [hp_X]/mL - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
    • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 200 [hp_C]/mL
    • CYNANCHUM VINCETOXICUM ROOT 6 [hp_X]/mL
    • EUPATORIUM PERFOLIATUM FLOWERING TOP 4 [hp_X]/mL
    • GELSEMIUM SEMPERVIRENS ROOT 3 [hp_X]/mL
    • INFLUENZA A VIRUS 12 [hp_X]/mL - The type species of the genus ALPHAINFLUENZAVIRUS that causes influenza and other diseases in humans and animals. Antigenic variation occurs frequently between strains, allowing classification into subtypes and variants. Transmission is usually by aerosol (human and most non-aquatic hosts) or waterborne (ducks). Infected birds shed the virus in their saliva, nasal secretions, and feces.
    • INFLUENZA B VIRUS 12 [hp_X]/mL - Species of the genus BETAINFLUENZAVIRUS that cause HUMAN INFLUENZA and other diseases primarily in humans. Antigenic variation is less extensive than in type A viruses (INFLUENZA A VIRUS) and consequently there is no basis for distinct subtypes or variants. Epidemics are less likely than with INFLUENZA A VIRUS and there have been no pandemics. Previously only found in humans, Influenza B virus has been isolated from seals which may constitute the animal reservoir from which humans are exposed.
    • PHOSPHORUS 5 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
    • SULFUR 4 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
    • ZINC 3 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.
    • ZINC GLUCONATE 3 [hp_X]/mL

    Which are Flu Terminator Drops UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Flu Terminator Drops Inactive Ingredients UNII Codes?

    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. The UNII codes for the inactive ingredients in this product are:

    Which are the Pharmacologic Classes for Flu Terminator Drops?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".