NDC 44911-0038 Anxiety

Aconitum Napellus,Arsenicum Album,Belladonna,Calcarea - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
44911-0038
Proprietary Name:
Anxiety
Non-Proprietary Name: [1]
Aconitum Napellus, Arsenicum Album, Belladonna, Calcarea Carbonica, Carcinosin, Causticum, Gelsemium Sempervirens, Lachesis Mutus, Mercurius Vivus, Nitricum Acidum, Phosphorus, Rhus Tox
Substance Name: [2]
Aconitum Napellus; Arsenic Trioxide; Atropa Belladonna; Causticum; Gelsemium Sempervirens Root; Human Breast Tumor Cell; Lachesis Muta Venom; Mercury; Nitric Acid; Oyster Shell Calcium Carbonate, Crude; Phosphorus; Toxicodendron Pubescens Leaf
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Energique, Inc.
    Labeler Code:
    44911
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-16-2012
    End Marketing Date: [10]
    08-10-2026
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 44911-0038-1

    Package Description: 30 mL in 1 BOTTLE, SPRAY

    Product Details

    What is NDC 44911-0038?

    The NDC code 44911-0038 is assigned by the FDA to the product Anxiety which is a human over the counter drug product labeled by Energique, Inc.. The generic name of Anxiety is aconitum napellus, arsenicum album, belladonna, calcarea carbonica, carcinosin, causticum, gelsemium sempervirens, lachesis mutus, mercurius vivus, nitricum acidum, phosphorus, rhus tox. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 44911-0038-1 30 ml in 1 bottle, spray . 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 Anxiety?

    May temporarily relieve fearfulness, restlessness, and fear of death and dying.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve fearfulness, restlessness, and fear of death and dying.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

    What are Anxiety 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 30 [hp_C]/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.
    • ARSENIC TRIOXIDE 30 [hp_C]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
    • ATROPA BELLADONNA 30 [hp_C]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
    • CAUSTICUM 30 [hp_C]/mL
    • GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/mL
    • HUMAN BREAST TUMOR CELL 30 [hp_C]/mL
    • LACHESIS MUTA VENOM 30 [hp_C]/mL
    • MERCURY 30 [hp_C]/mL - A silver metallic element that exists as a liquid at room temperature. It has the atomic symbol Hg (from hydrargyrum, liquid silver), atomic number 80, and atomic weight 200.59. Mercury is used in many industrial applications and its salts have been employed therapeutically as purgatives, antisyphilitics, disinfectants, and astringents. It can be absorbed through the skin and mucous membranes which leads to MERCURY POISONING. Because of its toxicity, the clinical use of mercury and mercurials is diminishing.
    • NITRIC ACID 30 [hp_C]/mL - Nitric acid (HNO3). A colorless liquid that is used in the manufacture of inorganic and organic nitrates and nitro compounds for fertilizers, dye intermediates, explosives, and many different organic chemicals. Continued exposure to vapor may cause chronic bronchitis; chemical pneumonitis may occur. (From Merck Index, 11th ed)
    • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
    • PHOSPHORUS 30 [hp_C]/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.
    • TOXICODENDRON PUBESCENS LEAF 30 [hp_C]/mL

    Which are Anxiety UNII Codes?

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

    Which are Anxiety 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:

    * 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.

    [10] 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.

    [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".