NDC 55714-2584 Allergies

Apis Mellifica,Echinacea,Hydrastis Canadensis,Taraxacum Officinale,Aconitum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
Proprietary Name:
Non-Proprietary Name: [1]
Apis Mellifica, Echinacea, Hydrastis Canadensis, Taraxacum Officinale, Aconitum Napellus, Aethusa Cynapium, Agaricus Muscarius, Aletris Farinosa, Alfalfa, Allium Cepa, Allium Sativum, Ambrosia Artemisiaefolia, Arsenicum Album, Artemisia Vulgaris, Arundo Mauritanica, Avena Sativa, Belladonna, Bellis Perrenis, Bovista, Bromium, Bryonia, Caffeinum, Calcarea Carbonica, Calluna Vulgaris, Flos, Capsicum Annuum, Cat Hair, Chamomilla, Chelidonium Majus, Chenopodium Anthelminticum, Cinnamomum
Substance Name: [2]
Abrus Precatorius Seed; Aconitum Napellus; Aethusa Cynapium; Aletris Farinosa Root; Alfalfa; Allylthiourea; Alpine Strawberry; Amanita Muscaria Fruiting Body; Ambrosia Artemisiifolia; Anacardium Occidentale Fruit; Anemone Pulsatilla; Apis Mellifera; Arsenic Trioxide; Artemisia Vulgaris Root; Arundo Pliniana Root; Ascorbic Acid; Astacus Astacus; Atropa Belladonna; Avena Sativa Flowering Top; Bellis Perennis; Black Mustard Seed; Bromine; Bryonia Alba Root; Caffeine; Calluna Vulgaris Flowering Top; Canis Lupus Familiaris Hair; Capsicum; Chelidonium Majus; Cinnamon; Claviceps Purpurea Sclerotium; Corn Silk; Cow Milk; Cynara Scolymus Leaf; Datura Stramonium; Drosera Anglica; Dysphania Ambrosioides; Echinacea, Unspecified; Egg Shell, Cooked; Elymus Repens Root; Euphrasia Stricta; Fagopyrum Esculentum; Fagus Sylvatica Nut; Felis Catus Hair; Fraxinus Americana Bark; Garlic; Gelsemium Sempervirens Root; Ginger; Glycyrrhiza Glabra; Goldenseal; Helianthemum Canadense; Histamine Dihydrochloride; House Dust; Hyoscyamus Niger; Juglans Regia Leaf; Juniperus Virginiana Twig; Lactose, Unspecified Form; Lilium Lancifolium Whole Flowering; Lycoperdon Utriforme Fruiting Body; Lycopodium Clavatum Spore; Lycopus Virginicus; Matricaria Chamomilla; Mentha Piperita; Nutmeg; Onion; Onosmodium Virginianum; Oyster Shell Calcium Carbonate, Crude; Parthenium Hysterophorus; Phytolacca Americana Root; Populus Balsamifera Leaf Bud; Populus Tremuloides Leaf; Potassium Iodide; Protortonia Cacti; Ptelea Trifoliata Bark; Quercus Robur Nut; Rhododendron Tomentosum Leafy Twig; Rosa X Damascena Flowering Top; Saccharin; Saccharomyces Cerevisiae; Salix Nigra Bark; Sambucus Nigra Flowering Top; Sanguinaria Canadensis Root; Schoenocaulon Officinale Seed; Sodium Chloride; Sodium Nitrate; Solanum Dulcamara Top; Solanum Lycopersicum; Solanum Nigrum Whole; Solanum Tuberosum; Sucrose; Sulfur; Taraxacum Officinale; Tobacco Leaf; Toxicodendron Pubescens Leaf; Trillium Erectum Root; Ulmus Rubra Bark; Urtica Urens; Ustilago Maydis; Wyethia Helenioides Root; Xerophyllum Asphodeloides; Yucca Filamentosa
NDC Directory Status:
Human Otc Drug
Product Type: [3]
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 Code:
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    Listing Expiration Date: [11]
    Exclude Flag: [12]
    Code Navigator:

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    Product Details

    What is NDC 55714-2584?

    The NDC code 55714-2584 is assigned by the FDA to the product Allergies which is a human over the counter drug product labeled by Newton Laboratories, Inc.. The generic name of Allergies is apis mellifica, echinacea, hydrastis canadensis, taraxacum officinale, aconitum napellus, aethusa cynapium, agaricus muscarius, aletris farinosa, alfalfa, allium cepa, allium sativum, ambrosia artemisiaefolia, arsenicum album, artemisia vulgaris, arundo mauritanica, avena sativa, belladonna, bellis perrenis, bovista, bromium, bryonia, caffeinum, calcarea carbonica, calluna vulgaris, flos, capsicum annuum, cat hair, chamomilla, chelidonium majus, chenopodium anthelminticum, cinnamomum. 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 55714-2584-1 30 ml in 1 bottle, glass . 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 Allergies?

    Formulated for symptoms associated with food and environmental allergens such as congestion, swollen glands, runny nose, cough, rashes and stomach upset.

    What are Allergies 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.

    Which are Allergies UNII Codes?

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

    Which are Allergies 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 Allergies?

    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".