F12 Solution/ Drops
NDC 63479-0612

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0612?
  4. F12 Pstvty Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

F12 (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 UNAPPROVED HOMEOPATHIC-approved product labeled by Apex Energetics Inc.. This medication is typically used as a allergens [cs]. It is supplied as a solution/ drops for sublingual administration. This product entry covers the primary NDC 63479-0612 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
63479-0612
Proprietary Name:
F12 Pstvty
Non-Proprietary Name: [1]
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
Substance Name: [2]
Aloe Vera Flower; Anethum Graveolens Whole; Berberis Aquifolium Whole; Calochortus Tolmiei Whole; Chamomile; Corn Silk; Fagus Sylvatica Flowering Top; Gold; Hypericum Perforatum Flower; Ilex Aquifolium Flowering Top; Ipomoea Purpurea Top; Jacaranda Caroba Flower; Juglans Regia Flowering Top; Lavandula Angustifolia Subsp. Angustifolia Flower; Lycopodium Clavatum Spore; Madia Elegans Whole; Monardella Odoratissima Whole; Naja Naja Venom; Nelumbo Nucifera Flower; Penstemon Davidsonii Whole; Persea Americana Whole; Phosphorus; Primula Hendersonii Whole; Prunus Persica Var. Nucipersica Whole; Pulsatilla Vulgaris Whole; Rosa Californica Whole; Salix Alba Flowering Top; Sarsaparilla; Scabies Lesion Lysate (human); Silene Laciniata Whole; Silver; Solidago Californica Whole; Tradescantia Occidentalis Whole; Trifolium Pratense Flower
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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 & Regulatory Data

Labeler Name: [5]
Apex Energetics Inc.
Labeler Code:
63479
Product Label ID:
bca474fe-2bcf-e7d3-e053-2a95a90a49af
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
03-12-1996
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 63479-0612?

The NDC code 63479-0612 is assigned by the FDA to the product F12 Pstvty. It is commonly known by its generic 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. This pharmaceutical product is labeled by Apex Energetics Inc. and is currently categorized as listed product. The medication is a solution/ drops administered via sublingual route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63479-0612-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

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 Active Ingredients of this product?

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 the associated UNII Codes?

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

  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM)
  • NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (Active Moiety)
  • PHOSPHORUS (UNII: 27YLU75U4W)
  • PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
  • PRUNUS PERSICA VAR. NUCIPERSICA WHOLE (UNII: F0503JK1C3)
  • PRUNUS PERSICA VAR. NUCIPERSICA WHOLE (UNII: F0503JK1C3) (Active Moiety)
  • PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV)
  • PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (Active Moiety)
  • TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
  • TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (Active Moiety)
  • NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)
  • NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV) (Active Moiety)
  • PERSEA AMERICANA WHOLE (UNII: 9W8ZP67K1Z)
  • PERSEA AMERICANA WHOLE (UNII: 9W8ZP67K1Z) (Active Moiety)
  • ALOE VERA FLOWER (UNII: 575DY8C1ER)
  • ALOE VERA FLOWER (UNII: 575DY8C1ER) (Active Moiety)
  • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U)
  • FAGUS SYLVATICA FLOWERING TOP (UNII: 21AF0IHY5U) (Active Moiety)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
  • JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
  • CORN SILK (UNII: 7D3VB244UX)
  • CORN SILK (UNII: 7D3VB244UX) (Active Moiety)
  • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
  • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) (Active Moiety)
  • SARSAPARILLA (UNII: 2H1576D5WG)
  • SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
  • TRADESCANTIA OCCIDENTALIS WHOLE (UNII: Z2H9Z91B2D)
  • TRADESCANTIA OCCIDENTALIS WHOLE (UNII: Z2H9Z91B2D) (Active Moiety)
  • ROSA CALIFORNICA WHOLE (UNII: H14X4P9EKJ)
  • ROSA CALIFORNICA WHOLE (UNII: H14X4P9EKJ) (Active Moiety)
  • SILVER (UNII: 3M4G523W1G)
  • SILVER (UNII: 3M4G523W1G) (Active Moiety)
  • GOLD (UNII: 79Y1949PYO)
  • GOLD (UNII: 79Y1949PYO) (Active Moiety)
  • ANETHUM GRAVEOLENS WHOLE (UNII: BWN6849791)
  • ANETHUM GRAVEOLENS WHOLE (UNII: BWN6849791) (Active Moiety)
  • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W)
  • ILEX AQUIFOLIUM FLOWERING TOP (UNII: 5ENR9SAN1W) (Active Moiety)
  • CALOCHORTUS TOLMIEI WHOLE (UNII: 831MXG026J)
  • CALOCHORTUS TOLMIEI WHOLE (UNII: 831MXG026J) (Active Moiety)
  • JACARANDA CAROBA FLOWER (UNII: 0JTX26L7CL)
  • JACARANDA CAROBA FLOWER (UNII: 0JTX26L7CL) (Active Moiety)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
  • LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
  • MADIA ELEGANS WHOLE (UNII: 9E097HJ37D)
  • MADIA ELEGANS WHOLE (UNII: 9E097HJ37D) (Active Moiety)
  • IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O)
  • IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O) (Active Moiety)
  • CHAMOMILE (UNII: FGL3685T2X)
  • CHAMOMILE (UNII: FGL3685T2X) (Active Moiety)
  • SOLIDAGO CALIFORNICA WHOLE (UNII: C72J9V97H5)
  • SOLIDAGO CALIFORNICA WHOLE (UNII: C72J9V97H5) (Active Moiety)
  • SILENE LACINIATA WHOLE (UNII: 565ZR7YWT0)
  • SILENE LACINIATA WHOLE (UNII: 565ZR7YWT0) (Active Moiety)
  • HYPERICUM PERFORATUM FLOWER (UNII: A6V4CUE7PV)
  • HYPERICUM PERFORATUM FLOWER (UNII: A6V4CUE7PV) (Active Moiety)
  • PRIMULA HENDERSONII WHOLE (UNII: 05P93760L4)
  • PRIMULA HENDERSONII WHOLE (UNII: 05P93760L4) (Active Moiety)
  • MONARDELLA ODORATISSIMA WHOLE (UNII: 85HVU818II)
  • MONARDELLA ODORATISSIMA WHOLE (UNII: 85HVU818II) (Active Moiety)
  • BERBERIS AQUIFOLIUM WHOLE (UNII: J4WG1JVR05)
  • BERBERIS AQUIFOLIUM WHOLE (UNII: J4WG1JVR05) (Active Moiety)
  • PENSTEMON DAVIDSONII WHOLE (UNII: 8K9DCX606Z)
  • PENSTEMON DAVIDSONII WHOLE (UNII: 8K9DCX606Z) (Active Moiety)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4)
  • SCABIES LESION LYSATE (HUMAN) (UNII: 5UAU16Z1U4) (Active Moiety)
  • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
  • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)

Which are the Inactive Ingredients associated 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 of this product?

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.

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Product & Regulatory Definitions
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.
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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".