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NDC 63479-0603 F03 Fr-rls

Aspen,Arsenicum Album,Diplacus Aurantiacus,Garlic,Lilium Tigrinum,Loquat,Luffa - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0603?
  4. F03 Fr-rls Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
63479-0603
Proprietary Name:
F03 Fr-rls
Non-Proprietary Name: [1]
Aspen, Arsenicum Album, Diplacus Aurantiacus, Garlic, Lilium Tigrinum, Loquat, Luffa Operculata, Mimulus Guttatus, Penstemon Davidsonii, Prunus Cerasifera, Red Horse Chestnut, Rubus Ursinus, Rockrose, Toxicodendron Diversilobum, Viola Odorata, Watermelon, Yellow Jasmine
Substance Name: [2]
Aesculus Carnea Flower; Allium Sativum Whole; Arsenic Trioxide; Diplacus Aurantiacus Whole; Eriobotrya Japonica Whole; Gelsemium Sempervirens Root; Helianthemum Nummularium Flower; Lilium Lancifolium Whole Flowering; Luffa Operculata Fruit; Mimulus Guttatus Flowering Top; Penstemon Davidsonii Whole; Populus Tremula Flowering Top; Prunus Cerasifera Flower; Rubus Ursinus Whole; Toxicodendron Diversilobum Whole; Viola Odorata Flower; Watermelon
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:
    bccede22-e48f-52bc-e053-2995a90a6d0f
    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 63479-0603?

    The NDC code 63479-0603 is assigned by the FDA to the product F03 Fr-rls which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F03 Fr-rls is aspen, arsenicum album, diplacus aurantiacus, garlic, lilium tigrinum, loquat, luffa operculata, mimulus guttatus, penstemon davidsonii, prunus cerasifera, red horse chestnut, rubus ursinus, rockrose, toxicodendron diversilobum, viola odorata, watermelon, yellow jasmine. 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 63479-0603-1 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 F03 Fr-rls?

    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 F03 Fr-rls 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 F03 Fr-rls UNII Codes?

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

    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • VIOLA ODORATA FLOWER (UNII: 438W01FC7A)
    • VIOLA ODORATA FLOWER (UNII: 438W01FC7A) (Active Moiety)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
    • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
    • ERIOBOTRYA JAPONICA WHOLE (UNII: 2FCJ9QNJ7O)
    • ERIOBOTRYA JAPONICA WHOLE (UNII: 2FCJ9QNJ7O) (Active Moiety)
    • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
    • LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
    • MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU)
    • MIMULUS GUTTATUS FLOWERING TOP (UNII: 192426I5JU) (Active Moiety)
    • TOXICODENDRON DIVERSILOBUM WHOLE (UNII: 9211E5735B)
    • TOXICODENDRON DIVERSILOBUM WHOLE (UNII: 9211E5735B) (Active Moiety)
    • PENSTEMON DAVIDSONII WHOLE (UNII: 8K9DCX606Z)
    • PENSTEMON DAVIDSONII WHOLE (UNII: 8K9DCX606Z) (Active Moiety)
    • AESCULUS CARNEA FLOWER (UNII: 717DPT98VM)
    • AESCULUS CARNEA FLOWER (UNII: 717DPT98VM) (Active Moiety)
    • RUBUS URSINUS WHOLE (UNII: EB3AN7DKSL)
    • RUBUS URSINUS WHOLE (UNII: EB3AN7DKSL) (Active Moiety)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
    • ALLIUM SATIVUM WHOLE (UNII: IIF21WT8O3)
    • ALLIUM SATIVUM WHOLE (UNII: IIF21WT8O3) (Active Moiety)
    • POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ)
    • POPULUS TREMULA FLOWERING TOP (UNII: 5Q01F7TPJJ) (Active Moiety)
    • DIPLACUS AURANTIACUS WHOLE (UNII: TO6G4140YA)
    • DIPLACUS AURANTIACUS WHOLE (UNII: TO6G4140YA) (Active Moiety)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
    • WATERMELON (UNII: 231473QB6R)
    • WATERMELON (UNII: 231473QB6R) (Active Moiety)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI)
    • LILIUM LANCIFOLIUM WHOLE FLOWERING (UNII: X67Z2963PI) (Active Moiety)

    Which are F03 Fr-rls 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 F03 Fr-rls?

    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".