F26 Prsvr

Allium Cepa Whole, Apis Mellifica, Aurum Metallicum, Borage, Bromus Ramosus, California Wildrose Whole, English Elm Ing Twig, English Hawthron, English Oak, European Hornbeam, European Olive, Gentianella Amarella, Gorse, Larix Decidua, Luffa Operculata, Mercurius Solubilis, Mullein, Natrum Muriaticum, Penstemon Davidsonii Whole, Platinum Metallicum, Pulsatilla Vulgaris, Purple Loosestrife Whole, Rosa Chinensis, Scotch Broom, Sepia, Wild Mustard, Yerba Santa, Zincum Metallicum


Apex Energetics Inc.
Human Otc Drug
NDC 63479-0626
F26 Prsvr also known as Allium Cepa Whole, Apis Mellifica, Aurum Metallicum, Borage, Bromus Ramosus, California Wildrose Whole, English Elm Ing Twig, English Hawthron, English Oak, European Hornbeam, European Olive, Gentianella Amarella, Gorse, Larix Decidua, Luffa Operculata, Mercurius Solubilis, Mullein, Natrum Muriaticum, Penstemon Davidsonii Whole, Platinum Metallicum, Pulsatilla Vulgaris, Purple Loosestrife Whole, Rosa Chinensis, Scotch Broom, Sepia, Wild Mustard, Yerba Santa, Zincum Metallicum is a human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for F26 Prsvr is 63479-0626. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in F26 Prsvr drug includes Allium Cepa Whole - 12 [hp_C]/mL Apis Mellifera - 15 [hp_X]/mL Borago Officinalis Flower - 12 [hp_C]/mL Bromus Ramosus Flower - 12 [hp_C]/mL Carpinus Betulus Flower - 12 [hp_C]/mL Crataegus Monogyna Flower - 12 [hp_C]/mL Cytisus Scoparius Flower - 12 [hp_C]/mL Eriodictyon Californicum Flowering Top - 12 [hp_C]/mL Gentianella Amarella Flower - 12 [hp_C]/mL Gold - 12 [hp_C]/mL and more. The currest status of F26 Prsvr drug is Active.

Drug Information:

Drug NDC: 63479-0626
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: F26 Prsvr
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: F26
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: PRSVR
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Allium Cepa Whole, Apis Mellifica, Aurum Metallicum, Borage, Bromus Ramosus, California Wildrose Whole, English Elm Ing Twig, English Hawthron, English Oak, European Hornbeam, European Olive, Gentianella Amarella, Gorse, Larix Decidua, Luffa Operculata, Mercurius Solubilis, Mullein, Natrum Muriaticum, Penstemon Davidsonii Whole, Platinum Metallicum, Pulsatilla Vulgaris, Purple Loosestrife Whole, Rosa Chinensis, Scotch Broom, Sepia, Wild Mustard, Yerba Santa, Zincum Metallicum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Apex Energetics Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Solution/ Drops
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:ALLIUM CEPA WHOLE - 12 [hp_C]/mL
APIS MELLIFERA - 15 [hp_X]/mL
BORAGO OFFICINALIS FLOWER - 12 [hp_C]/mL
BROMUS RAMOSUS FLOWER - 12 [hp_C]/mL
CARPINUS BETULUS FLOWER - 12 [hp_C]/mL
CRATAEGUS MONOGYNA FLOWER - 12 [hp_C]/mL
CYTISUS SCOPARIUS FLOWER - 12 [hp_C]/mL
ERIODICTYON CALIFORNICUM FLOWERING TOP - 12 [hp_C]/mL
GENTIANELLA AMARELLA FLOWER - 12 [hp_C]/mL
GOLD - 12 [hp_C]/mL
LARIX DECIDUA FLOWERING TOP - 12 [hp_C]/mL
LUFFA OPERCULATA FRUIT - 12 [hp_C]/mL
LYTHRUM SALICARIA WHOLE - 12 [hp_C]/mL
MERCURIUS SOLUBILIS - 15 [hp_X]/mL
OLEA EUROPAEA FLOWER - 12 [hp_C]/mL
PENSTEMON DAVIDSONII WHOLE - 12 [hp_C]/mL
PLATINUM - 15 [hp_X]/mL
PULSATILLA VULGARIS - 15 [hp_X]/mL
QUERCUS ROBUR FLOWER - 12 [hp_C]/mL
ROSA CALIFORNICA WHOLE - 12 [hp_C]/mL
ROSA CHINENSIS FLOWER - 12 [hp_C]/mL
SEPIA OFFICINALIS JUICE - 12 [hp_C]/mL
SINAPIS ARVENSIS FLOWERING/FRUITING TOP - 12 [hp_C]/mL
SODIUM CHLORIDE - 15 [hp_X]/mL
ULEX EUROPAEUS FLOWER - 12 [hp_C]/mL
ULMUS PROCERA FLOWERING TWIG - 12 [hp_C]/mL
VERBASCUM DENSIFLORUM FLOWER - 12 [hp_C]/mL
ZINC - 12 [hp_C]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:SUBLINGUAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 12 Mar, 1996
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 13 Jun, 2026
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.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Apex Energetics Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UPC:0818960011994
UPC stands for Universal Product Code.
NUI:N0000185021
N0000175629
N0000184306
N0000185001
M0000728
M0002274
N0000185508
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:8P2VLG2456
7S82P3R43Z
7X23S1OW1N
0W9O574LE8
07YL55QKZ9
NT52AMP29J
205JZ3JIKD
HKE3DK7994
ZKH2SOY1AR
79Y1949PYO
9UMZ642257
C4MO6809HU
E9O9E4Q192
324Y4038G2
498M34P1VZ
8K9DCX606Z
49DFR088MY
I76KB35JEV
ML644HED2V
H14X4P9EKJ
QH060TH2D2
QDL83WN8C2
WWX61E1ZAK
451W47IQ8X
398DBS1PXN
J3O020I532
N7FC535Q3R
J41CSQ7QDS
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:Standardized Insect Venom Allergenic Extract [EPC]
Standardized Chemical Allergen [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:Allergens [CS]
Bee Venoms [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Allergens [CS]
Bee Venoms [CS]
Cell-mediated Immunity [PE]
Increased Histamine Release [PE]
Increased IgG Production [PE]
Increased Large Intestinal Motility [PE]
Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
Osmotic Activity [MoA]
Osmotic Laxative [EPC]
Standardized Chemical Allergen [EPC]
Standardized Insect Venom Allergenic Extract [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63479-0626-130 mL in 1 BOTTLE, GLASS (63479-0626-1)12 Mar, 1996N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Uses: for temporary relief of minor: exhaustion* lack of endurance* apathy* easily discouraged* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

F26 prsvr allium cepa whole, apis mellifica, aurum metallicum, borage, bromus ramosus, california wildrose whole, english elm ing twig, english hawthron, english oak, european hornbeam, european olive, gentianella amarella, gorse, larix decidua, luffa operculata, mercurius solubilis, mullein, natrum muriaticum, penstemon davidsonii whole, platinum metallicum, pulsatilla vulgaris, purple loosestrife whole, rosa chinensis, scotch broom, sepia, wild mustard, yerba santa, zincum metallicum zinc zinc alcohol water gold gold eriodictyon californicum flowering top eriodictyon californicum flowering top allium cepa whole allium cepa whole mercurius solubilis mercurius solubilis verbascum densiflorum flower verbascum densiflorum flower platinum platinum rosa chinensis flower rosa chinensis flower sodium chloride sodium cation gentianella amarella flower gentianella amarella flower ulex europaeus flower ulex europaeus flower larix decidua flowering top larix decidua flowering top luffa operculata fruit luffa operculata fruit penstemon davidsonii whole penstemon davidsonii whole pulsatilla vulgaris pulsatilla vulgaris rosa californica whole rosa californica whole ulmus procera flowering twig ulmus procera flowering twig crataegus monogyna flower crataegus monogyna flower olea europaea flower olea europaea flower sepia officinalis juice sepia officinalis juice sinapis arvensis flowering/fruiting top sinapis arvensis flowering/fruiting top quercus robur flower quercus robur flower lythrum salicaria whole lythrum salicaria whole cytisus scoparius flower cytisus scoparius flower apis mellifera apis mellifera borago officinalis flower borago officinalis flower bromus ramosus flower bromus ramosus flower carpinus betulus flower carpinus betulus flower

Indications and Usage:

Uses: for temporary relief of minor: exhaustion* lack of endurance* apathy* easily discouraged* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Warnings:

Warnings: if pregnant or breastfeeding , ask a health professional before use. do not use if clear seal over the cap is broken or missing. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. stop use and ask a doctor if eexhaustion, lack of endurance, apathy, easily discouraged, or other symptoms do not improve within 7 days or are accompanied by fever.

Dosage and Administration:

Directions: 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.

Stop Use:

Stop use and ask a doctor if eexhaustion, lack of endurance, apathy, easily discouraged, or other symptoms do not improve within 7 days or are accompanied by fever.

Package Label Principal Display Panel:

Futureplex® f26 flower essences prsvr™ homeopathic formula exhaustion* lack of endurance* 1 fl oz (30 ml) alcohol 20% by volume f2621-0420

Further Questions:

Distributed by apex energetics. questions? 16592 hale ave., irvine, ca 92606, usa


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.