F12 Pstvty

Aloe Vera, Avocado, Berberis Aquifolium, Calochortus Tolmie, Caroba, Chamomile, Cornsilk, Dill, Fagus Sylvatica, Gold, Hypericum Perforatum, Ilex Aquifolium, Juglans Regia, Lavender, Lycopodium Clavatum, Madia Elegans, Meadia Hendersonii, Monardella, Morning Glory, Naja Tripudians, Penstemon Davidsonii, Phosphorus, Prunus Persica, Psorinum, Pulsatilla Vulgaris, Red Clover, Rosa Californica, Sacred Lotus, Sarsaparilla, Silene Laciniata, Silver, Solidago Californica, Spiderwort, White Willow

Apex Energetics Inc.
Human Otc Drug
NDC 63479-0612

F12 Pstvty also known as Aloe Vera, Avocado, Berberis Aquifolium, Calochortus Tolmie, Caroba, Chamomile, Cornsilk, Dill, Fagus Sylvatica, Gold, Hypericum Perforatum, Ilex Aquifolium, Juglans Regia, Lavender, Lycopodium Clavatum, Madia Elegans, Meadia Hendersonii, Monardella, Morning Glory, Naja Tripudians, Penstemon Davidsonii, Phosphorus, Prunus Persica, Psorinum, Pulsatilla Vulgaris, Red Clover, Rosa Californica, Sacred Lotus, Sarsaparilla, Silene Laciniata, Silver, Solidago Californica, Spiderwort, White Willow is a human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for F12 Pstvty is 63479-0612. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in F12 Pstvty drug includes Aloe Vera Flower - 12 [hp_C]/mL Anethum Graveolens Whole - 12 [hp_C]/mL Berberis Aquifolium Whole - 12 [hp_C]/mL Calochortus Tolmiei Whole - 12 [hp_C]/mL Chamomile - 12 [hp_C]/mL Corn Silk - 12 [hp_C]/mL Fagus Sylvatica Flowering Top - 12 [hp_C]/mL Gold - 12 [hp_C]/mL Hypericum Perforatum Flower - 12 [hp_C]/mL Ilex Aquifolium Flowering Top - 12 [hp_C]/mL and more. The currest status of F12 Pstvty drug is Active.

Drug Information:

Drug NDC:	63479-0612
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:	F12 Pstvty
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	F12
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	PSTVTY
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:	Aloe Vera, Avocado, Berberis Aquifolium, Calochortus Tolmie, Caroba, Chamomile, Cornsilk, Dill, Fagus Sylvatica, Gold, Hypericum Perforatum, Ilex Aquifolium, Juglans Regia, Lavender, Lycopodium Clavatum, Madia Elegans, Meadia Hendersonii, Monardella, Morning Glory, Naja Tripudians, Penstemon Davidsonii, Phosphorus, Prunus Persica, Psorinum, Pulsatilla Vulgaris, Red Clover, Rosa Californica, Sacred Lotus, Sarsaparilla, Silene Laciniata, Silver, Solidago Californica, Spiderwort, White Willow
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:	ALOE VERA FLOWER - 12 [hp_C]/mL ANETHUM GRAVEOLENS WHOLE - 12 [hp_C]/mL BERBERIS AQUIFOLIUM WHOLE - 12 [hp_C]/mL CALOCHORTUS TOLMIEI WHOLE - 12 [hp_C]/mL CHAMOMILE - 12 [hp_C]/mL CORN SILK - 12 [hp_C]/mL FAGUS SYLVATICA FLOWERING TOP - 12 [hp_C]/mL GOLD - 12 [hp_C]/mL HYPERICUM PERFORATUM FLOWER - 12 [hp_C]/mL ILEX AQUIFOLIUM FLOWERING TOP - 12 [hp_C]/mL Load more... IPOMOEA PURPUREA TOP - 12 [hp_C]/mL JACARANDA CAROBA FLOWER - 12 [hp_C]/mL JUGLANS REGIA FLOWERING TOP - 12 [hp_C]/mL LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER - 12 [hp_C]/mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_C]/mL MADIA ELEGANS WHOLE - 12 [hp_C]/mL MONARDELLA ODORATISSIMA WHOLE - 12 [hp_C]/mL NAJA NAJA VENOM - 12 [hp_C]/mL NELUMBO NUCIFERA FLOWER - 12 [hp_C]/mL PENSTEMON DAVIDSONII WHOLE - 12 [hp_C]/mL PERSEA AMERICANA WHOLE - 12 [hp_C]/mL PHOSPHORUS - 15 [hp_C]/mL PRIMULA HENDERSONII WHOLE - 12 [hp_C]/mL PRUNUS PERSICA VAR. NUCIPERSICA WHOLE - 12 [hp_C]/mL PULSATILLA VULGARIS WHOLE - 15 [hp_C]/mL ROSA CALIFORNICA WHOLE - 12 [hp_C]/mL SALIX ALBA FLOWERING TOP - 12 [hp_C]/mL SARSAPARILLA - 15 [hp_C]/mL SCABIES LESION LYSATE (HUMAN) - 12 [hp_C]/mL SILENE LACINIATA WHOLE - 12 [hp_C]/mL SILVER - 12 [hp_C]/mL SOLIDAGO CALIFORNICA WHOLE - 12 [hp_C]/mL TRADESCANTIA OCCIDENTALIS WHOLE - 12 [hp_C]/mL TRIFOLIUM PRATENSE FLOWER - 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:	20 Dec, 2025
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:	0818960011864
UPC stands for Universal Product Code.
NUI:	N0000185508 N0000175629 N0000184306 M0000728
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	575DY8C1ER BWN6849791 J4WG1JVR05 831MXG026J FGL3685T2X 7D3VB244UX 21AF0IHY5U 79Y1949PYO A6V4CUE7PV 5ENR9SAN1W Load more... XMQ0V9812O 0JTX26L7CL 3BA2N709NG 19AH1RAF4M C88X29Y479 9E097HJ37D 85HVU818II ZZ4AG7L7VM 61W322NLDV 8K9DCX606Z 9W8ZP67K1Z 27YLU75U4W 05P93760L4 F0503JK1C3 I76KB35JEV H14X4P9EKJ XBP5X7E70R 2H1576D5WG 5UAU16Z1U4 565ZR7YWT0 3M4G523W1G C72J9V97H5 Z2H9Z91B2D 4JS0838828
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 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]
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]
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] Cell-mediated Immunity [PE] Increased Histamine Release [PE] Standardized Chemical Allergen [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
63479-0612-1	30 mL in 1 BOTTLE, GLASS (63479-0612-1)	12 Mar, 1996	N/A	No
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.

Other medicines with the same generic name

F12 Pstvty

Aloe Vera & more..

Solution/ Drops
Apex Energetics Inc.
NDC: 63479-0612

Purpose:

Uses: for temporary relief of minor: melancholy* despair* abdominal pains* hopelessness* low-spiritedness* fearfulness* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

F12 pstvty aloe vera, avocado, berberis aquifolium, calochortus tolmie, caroba, chamomile, cornsilk, dill, fagus sylvatica, gold, hypericum perforatum, ilex aquifolium, juglans regia, lavender, lycopodium clavatum, madia elegans, meadia hendersonii, monardella, morning glory, naja tripudians, penstemon davidsonii, phosphorus, prunus persica, psorinum, pulsatilla vulgaris, red clover, rosa californica, sacred lotus, sarsaparilla, silene laciniata, silver, solidago californica, spiderwort, white willow naja naja venom naja naja venom phosphorus phosphorus prunus persica var. nucipersica whole prunus persica var. nucipersica whole pulsatilla vulgaris whole pulsatilla vulgaris whole trifolium pratense flower trifolium pratense flower nelumbo nucifera flower nelumbo nucifera flower persea americana whole persea americana whole aloe vera flower aloe vera flower fagus sylvatica flowering top fagus sylvatica flowering top juglans regia flowering top juglans regia flowering top corn silk corn silk lavandula angustifolia subsp. angustifolia flower lavandula angustifolia subsp. angustifolia flower sarsaparilla sarsaparilla tradescantia occidentalis whole tradescantia occidentalis whole rosa californica whole rosa californica whole silver silver gold gold anethum graveolens whole anethum graveolens whole ilex aquifolium flowering top ilex aquifolium flowering top calochortus tolmiei whole calochortus tolmiei whole alcohol water jacaranda caroba flower jacaranda caroba flower lycopodium clavatum spore lycopodium clavatum spore madia elegans whole madia elegans whole ipomoea purpurea top ipomoea purpurea top chamomile chamomile solidago californica whole solidago californica whole silene laciniata whole silene laciniata whole hypericum perforatum flower hypericum perforatum flower primula hendersonii whole primula hendersonii whole monardella odoratissima whole monardella odoratissima whole berberis aquifolium whole berberis aquifolium whole penstemon davidsonii whole penstemon davidsonii whole scabies lesion lysate (human) scabies lesion lysate (human) salix alba flowering top salix alba flowering top

Indications and Usage:

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 melancholy, despair, abdominal pains, hopelessness, low-spiritedness, fearfulness, 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 melancholy, despair, abdominal pains, hopelessness, low-spiritedness, fearfulness, or other symptoms do not improve within 7 days or are accompanied by fever.

Package Label Principal Display Panel:

FutureplexÂ® f12 flower essences pstvtyâ¢ homeopathic formula melancholy* despair* abdominal pains* 1 fl oz (30 ml) alcohol 20% by volume f1221-0727

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.