NDC 63479-0619 F19 Strng-mnd

Anacardium Orientale,Arnica Montana,Aurum Metallicum,Castanea Sativa,Citrus - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
63479-0619
Proprietary Name:
F19 Strng-mnd
Non-Proprietary Name: [1]
Anacardium Orientale, Arnica Montana, Aurum Metallicum, Castanea Sativa, Citrus Sinensis, Crataegus Monogyna, Cytisus Scoparius, Dandelion, Fagus Sylvatica, Fuchsia, Gorse, Hydrastis Canadensis, Ignatia Amara, Iron, Kali Phosphoricum, Malus Sylvestris, Natrum Muriaticum, Paeonia Californica, Pomegranate, Prunella Vulgaris, Rosa Californica, Sinapis Arvensis, Yarrow, Yerba Santa
Substance Name: [2]
Achillea Millefolium Flower; Arnica Montana; Arnica Montana Flower; Castanea Sativa Flower; Citrus Sinensis Flower; Crataegus Monogyna Flower; Cytisus Scoparius Flower; Eriodictyon Californicum Flowering Top; Fagus Sylvatica Flowering Top; Fuchsia Magellanica Whole; Gold; Hydrastis Canadensis Whole; Iron; Malus Sylvestris Flower; Paeonia Californica Whole; Potassium Phosphate, Dibasic; Prunella Vulgaris Flower; Punica Granatum Flower; Rosa Californica Whole; Semecarpus Anacardium Juice; Sinapis Arvensis Flowering/fruiting Top; Sodium Chloride; Strychnos Ignatii Seed; Taraxacum Officinale Flowering Top; Ulex Europaeus Flower
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • Sublingual - Administration beneath the tongue.
  • Labeler Code:
    63479
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-12-1996
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 63479-0619?

    The NDC code 63479-0619 is assigned by the FDA to the product F19 Strng-mnd which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F19 Strng-mnd is anacardium orientale, arnica montana, aurum metallicum, castanea sativa, citrus sinensis, crataegus monogyna, cytisus scoparius, dandelion, fagus sylvatica, fuchsia, gorse, hydrastis canadensis, ignatia amara, iron, kali phosphoricum, malus sylvestris, natrum muriaticum, paeonia californica, pomegranate, prunella vulgaris, rosa californica, sinapis arvensis, yarrow, yerba santa. The product's dosage form is solution/ drops and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-0619-1 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 F19 Strng-mnd?

    Adults & children ages 12 years and over: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age

    What are F19 Strng-mnd 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 F19 Strng-mnd UNII Codes?

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

    • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
    • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (Active Moiety)
    • IRON (UNII: E1UOL152H7)
    • IRON (UNII: E1UOL152H7) (Active Moiety)
    • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
    • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
    • SODIUM CHLORIDE (UNII: 451W47IQ8X)
    • SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
    • PUNICA GRANATUM FLOWER (UNII: D9B634V4GP)
    • PUNICA GRANATUM FLOWER (UNII: D9B634V4GP) (Active Moiety)
    • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK)
    • SINAPIS ARVENSIS FLOWERING/FRUITING TOP (UNII: WWX61E1ZAK) (Active Moiety)
    • ACHILLEA MILLEFOLIUM FLOWER (UNII: YQR8R0SQEA)
    • ACHILLEA MILLEFOLIUM FLOWER (UNII: YQR8R0SQEA) (Active Moiety)
    • PAEONIA CALIFORNICA WHOLE (UNII: 38QL9598DU)
    • PAEONIA CALIFORNICA WHOLE (UNII: 38QL9598DU) (Active Moiety)
    • MALUS SYLVESTRIS FLOWER (UNII: 6ZJ8N1924Z)
    • MALUS SYLVESTRIS FLOWER (UNII: 6ZJ8N1924Z) (Active Moiety)
    • PRUNELLA VULGARIS FLOWER (UNII: AT1FD041EF)
    • PRUNELLA VULGARIS FLOWER (UNII: AT1FD041EF) (Active Moiety)
    • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3)
    • CASTANEA SATIVA FLOWER (UNII: YHZ719F7M3) (Active Moiety)
    • CITRUS SINENSIS FLOWER (UNII: H02N5LQ5F6)
    • CITRUS SINENSIS FLOWER (UNII: H02N5LQ5F6) (Active Moiety)
    • TARAXACUM OFFICINALE FLOWERING TOP (UNII: DQS85W46HV)
    • TARAXACUM OFFICINALE FLOWERING TOP (UNII: DQS85W46HV) (Active Moiety)
    • ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN)
    • ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN) (Active Moiety)
    • POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
    • POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
    • CYTISUS SCOPARIUS FLOWER (UNII: 205JZ3JIKD)
    • CYTISUS SCOPARIUS FLOWER (UNII: 205JZ3JIKD) (Active Moiety)
    • ERIODICTYON CALIFORNICUM FLOWERING TOP (UNII: HKE3DK7994)
    • ERIODICTYON CALIFORNICUM FLOWERING TOP (UNII: HKE3DK7994) (Active Moiety)
    • CRATAEGUS MONOGYNA FLOWER (UNII: NT52AMP29J)
    • CRATAEGUS MONOGYNA FLOWER (UNII: NT52AMP29J) (Active Moiety)
    • HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
    • HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T) (Active Moiety)
    • SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
    • SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
    • ARNICA MONTANA (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • GOLD (UNII: 79Y1949PYO)
    • GOLD (UNII: 79Y1949PYO) (Active Moiety)
    • ROSA CALIFORNICA WHOLE (UNII: H14X4P9EKJ)
    • ROSA CALIFORNICA WHOLE (UNII: H14X4P9EKJ) (Active Moiety)
    • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
    • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
    • FUCHSIA MAGELLANICA WHOLE (UNII: J66MJH220L)
    • FUCHSIA MAGELLANICA WHOLE (UNII: J66MJH220L) (Active Moiety)

    Which are F19 Strng-mnd 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 F19 Strng-mnd?

    * 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".