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  4. NDC Product Code: 63479-0608 F08 Frgv

NDC 63479-0608 F08 Frgv

Allegheny Monkeyflower,Arnica Montana,Arnica Montana Flower,Ceanothus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0608?
  4. F08 Frgv Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
63479-0608
Proprietary Name:
F08 Frgv
Non-Proprietary Name: [1]
Allegheny Monkeyflower, Arnica Montana, Arnica Montana Flower, Ceanothus Integerrimus, Ehrendorferia Chrysantha, Fagus Sylvatica Flower, Ignatia Amara, Ilex Aquifolium Flower, Malus Sylvestris Flower, Mullein Flower, Nettleleaf Giant Hyssop, Pinus Sylvestris Flower, Salix Alba Flower
Substance Name: [2]
Agastache Urticifolia Whole; Arnica Montana; Arnica Montana Flower; Ceanothus Integerrimus Whole; Ehrendorferia Chrysantha Whole; Fagus Sylvatica Flowering Top; Ilex Aquifolium Flowering Top; Malus Sylvestris Flower; Mimulus Ringens Whole; Pinus Sylvestris Flowering Top; Salix Alba Flowering Top; Strychnos Ignatii Seed; Verbascum Densiflorum 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 Name: [5]
    Apex Energetics Inc.
    Labeler Code:
    63479
    Product Label ID:
    bc91d5bd-fa6e-8245-e053-2995a90a3e8c
    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
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 63479-0608?

    The NDC code 63479-0608 is assigned by the FDA to the product F08 Frgv which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F08 Frgv is allegheny monkeyflower, arnica montana, arnica montana flower, ceanothus integerrimus, ehrendorferia chrysantha, fagus sylvatica flower, ignatia amara, ilex aquifolium flower, malus sylvestris flower, mullein flower, nettleleaf giant hyssop, pinus sylvestris flower, salix alba flower. 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 63479-0608-1 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 F08 Frgv?

    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 F08 Frgv 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 F08 Frgv UNII Codes?

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

    • PINUS SYLVESTRIS FLOWERING TOP (UNII: 2HEM73YI9I)
    • PINUS SYLVESTRIS FLOWERING TOP (UNII: 2HEM73YI9I) (Active Moiety)
    • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
    • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)
    • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
    • STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
    • VERBASCUM DENSIFLORUM FLOWER (UNII: N7FC535Q3R)
    • VERBASCUM DENSIFLORUM FLOWER (UNII: N7FC535Q3R) (Active Moiety)
    • AGASTACHE URTICIFOLIA WHOLE (UNII: 8A94843BM7)
    • AGASTACHE URTICIFOLIA WHOLE (UNII: 8A94843BM7) (Active Moiety)
    • MIMULUS RINGENS WHOLE (UNII: W4KH5N2DCK)
    • MIMULUS RINGENS WHOLE (UNII: W4KH5N2DCK) (Active Moiety)
    • MALUS SYLVESTRIS FLOWER (UNII: 6ZJ8N1924Z)
    • MALUS SYLVESTRIS FLOWER (UNII: 6ZJ8N1924Z) (Active Moiety)
    • ARNICA MONTANA (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
    • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (Active Moiety)
    • CEANOTHUS INTEGERRIMUS WHOLE (UNII: N76K76PTFU)
    • CEANOTHUS INTEGERRIMUS WHOLE (UNII: N76K76PTFU) (Active Moiety)
    • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W)
    • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W) (Active Moiety)
    • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
    • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
    • EHRENDORFERIA CHRYSANTHA WHOLE (UNII: 68HKD4QMJR)
    • EHRENDORFERIA CHRYSANTHA WHOLE (UNII: 68HKD4QMJR) (Active Moiety)

    Which are F08 Frgv 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.

    [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".