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  4. NDC Product Code: 63479-0625 F25 Lf-chngs

NDC 63479-0625 F25 Lf-chngs

Agrimony Flower Solution/ Drops Sublingual - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0625?
  4. F25 Lf-chngs Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
63479-0625
Proprietary Name:
F25 Lf-chngs
Non-Proprietary Name: [1]
Agrimony Flower
Substance Name: [2]
Aesculus Hippocastanum Flower; Agrimonia Eupatoria Flower; Arnica Montana Flower; Arsenic Trioxide; Artemisia Tridentata Whole; Calluna Vulgaris Flowering Top; Calochortus Tolmiei Whole; Capsicum; Dieffenbachia Seguine; Eschscholzia Californica Flower; Fagus Sylvatica Flowering Top; Gossypium Herbaceum Flower; Helianthus Annuus Flowering Top; Hylotelephium Telephium Whole; Ipomoea Purpurea Top; Juglans Regia Flowering Top; Lachesis Muta Venom; Larrea Tridentata Whole; Lavandula Angustifolia Subsp. Angustifolia Flower; Lawsonia Inermis Flowering Top; Lonicera Caprifolium Flower; Malva Neglecta Whole; Matricaria Chamomilla Flowering Top; Passiflora Incarnata Flowering Top; Penstemon Davidsonii Whole; Petunia Axillaris Whole; Plantago Major; Prunella Vulgaris Flower; Ranunculus Bulbosus Whole; Rosa Californica Whole; Salix Alba Flowering Top; Salvia Officinalis Flowering Top; Sepia Officinalis Juice; Silicon Dioxide; Strychnos Nux-vomica Seed
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:
    bf3c7a21-0e4e-6395-e053-2a95a90a7156
    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 Structure:
    Code Navigator:

    Product Packages

    NDC Code 63479-0625-1

    Package Description: 30 mL in 1 BOTTLE, GLASS

    Product Details

    What is NDC 63479-0625?

    The NDC code 63479-0625 is assigned by the FDA to the product F25 Lf-chngs which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of F25 Lf-chngs is agrimony 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 63479-0625-1 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 F25 Lf-chngs?

    Adults & children ages 12 years and over: Take 5-10 drops under the tongue 2-3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are F25 Lf-chngs 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 F25 Lf-chngs UNII Codes?

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

    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)
    • LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M) (Active Moiety)
    • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
    • SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)
    • ARTEMISIA TRIDENTATA WHOLE (UNII: 45E08M336T)
    • ARTEMISIA TRIDENTATA WHOLE (UNII: 45E08M336T) (Active Moiety)
    • RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB)
    • RANUNCULUS BULBOSUS WHOLE (UNII: AEQ8NXJ0MB) (Active Moiety)
    • DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B)
    • DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B) (Active Moiety)
    • ROSA CALIFORNICA WHOLE (UNII: H14X4P9EKJ)
    • ROSA CALIFORNICA WHOLE (UNII: H14X4P9EKJ) (Active Moiety)
    • MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02)
    • MATRICARIA CHAMOMILLA FLOWERING TOP (UNII: 3VNC7T6Z02) (Active Moiety)
    • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M)
    • AESCULUS HIPPOCASTANUM FLOWER (UNII: KK0Z92II8M) (Active Moiety)
    • CAPSICUM (UNII: 00UK7646FG)
    • CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
    • LARREA TRIDENTATA WHOLE (UNII: B755J144H1)
    • LARREA TRIDENTATA WHOLE (UNII: B755J144H1) (Active Moiety)
    • SALVIA OFFICINALIS FLOWERING TOP (UNII: 48JCS720FN)
    • SALVIA OFFICINALIS FLOWERING TOP (UNII: 48JCS720FN) (Active Moiety)
    • CALLUNA VULGARIS FLOWERING TOP (UNII: D9PC510CQV)
    • CALLUNA VULGARIS FLOWERING TOP (UNII: D9PC510CQV) (Active Moiety)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
    • STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
    • PENSTEMON DAVIDSONII WHOLE (UNII: 8K9DCX606Z)
    • PENSTEMON DAVIDSONII WHOLE (UNII: 8K9DCX606Z) (Active Moiety)
    • LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)
    • LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) (Active Moiety)
    • GOSSYPIUM HERBACEUM FLOWER (UNII: CVM893280N)
    • GOSSYPIUM HERBACEUM FLOWER (UNII: CVM893280N) (Active Moiety)
    • ESCHSCHOLZIA CALIFORNICA FLOWER (UNII: 7JX5YDQ0D6)
    • ESCHSCHOLZIA CALIFORNICA FLOWER (UNII: 7JX5YDQ0D6) (Active Moiety)
    • HYLOTELEPHIUM TELEPHIUM WHOLE (UNII: PH797NEU5T)
    • HYLOTELEPHIUM TELEPHIUM WHOLE (UNII: PH797NEU5T) (Active Moiety)
    • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2)
    • SEPIA OFFICINALIS JUICE (UNII: QDL83WN8C2) (Active Moiety)
    • HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
    • HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) (Active Moiety)
    • CALOCHORTUS TOLMIEI WHOLE (UNII: 831MXG026J)
    • CALOCHORTUS TOLMIEI WHOLE (UNII: 831MXG026J) (Active Moiety)
    • LAWSONIA INERMIS FLOWERING TOP (UNII: UF2093XE64)
    • LAWSONIA INERMIS FLOWERING TOP (UNII: UF2093XE64) (Active Moiety)
    • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
    • AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
    • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
    • ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (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)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I)
    • LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
    • IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O)
    • IPOMOEA PURPUREA TOP (UNII: XMQ0V9812O) (Active Moiety)
    • PETUNIA AXILLARIS WHOLE (UNII: B7U2BWH3OT)
    • PETUNIA AXILLARIS WHOLE (UNII: B7U2BWH3OT) (Active Moiety)
    • PLANTAGO MAJOR (UNII: W2469WNO6U)
    • PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
    • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
    • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
    • MALVA NEGLECTA WHOLE (UNII: S0QQA41760)
    • MALVA NEGLECTA WHOLE (UNII: S0QQA41760) (Active Moiety)
    • PRUNELLA VULGARIS FLOWER (UNII: AT1FD041EF)
    • PRUNELLA VULGARIS FLOWER (UNII: AT1FD041EF) (Active Moiety)
    • PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
    • PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O) (Active Moiety)

    Which are F25 Lf-chngs 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".