F25 Solution/ Drops
NDC Package 63479-0625-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

F25 (agrimony flower) solution/ dropses is 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. This formulation utilizes a solution/ drops delivery system. Marketed by Apex Energetics Inc., this product is identified by NDC 63479-0625.

Identification & Billing

NDC Package Code
63479-0625-1
Package Description
30 mL in 1 BOTTLE, GLASS
Product Code
63479-0625
11-Digit Billing Format
63479062501

Clinical Specifications

Proprietary Name
F25 Lf-chngs
Non-Proprietary Name
Agrimony Flower
Substance Name
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
Dosage Form
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route
Sublingual - Administration beneath the tongue.
Active Ingredient(s)
Pharmacologic Class
Usage Information
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.

Regulatory & Marketing

Labeler Name
Apex Energetics Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-12-1996
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 63479-0625-1 identifies a specific commercial package of 30 ml in 1 bottle, glass of F25 Lf-chngs, a human over the counter drug labeled by Apex Energetics Inc.. This solution/ drops is formulated for sublingual use and contains 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 as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Apex Energetics Inc. on March 12, 1996. The current certification is valid through December 31, 2026.

How is this Apex Energetics Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 63479062501. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
63479-0625-1
11-Digit CMS (5-4-2)
63479-0625-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.