N09 Solution/ Drops
NDC Package 63479-1409-1
Package Information
N09 (aconitum napellus, allium cepa, allium sativum, belladonna, calcarea sulphurica, calendula officinalis, echinacea angustifolia, ferrum phosphoricum, calcium sulfide, hydrastis canadensis, lachesis mutus, myristica sebifera, silicea, thuja occidentalis) solution/ dropses is adults & children ages 12 years and over: Take 10 drops under the tongue 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 63479-1409.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS 200 [hp_X]/mL
- ATROPA BELLADONNA 200 [hp_X]/mL
- CALCIUM SULFATE ANHYDROUS 60 [hp_X]/mL
- CALCIUM SULFIDE 200 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 60 [hp_X]/mL
- GARLIC 30 [hp_X]/mL
- GOLDENSEAL 1 [hp_X]/mL
- LACHESIS MUTA VENOM 90 [hp_X]/mL
- ONION 30 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 90 [hp_X]/mL
- VIROLA SEBIFERA RESIN 2 [hp_X]/mL
- Allergens - [CS]
- Allergens - [CS]
- Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
- Calcium - [CS]
- Cations, Divalent - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Phosphate Binder - [EPC] (Established Pharmacologic Class)
- Phosphate Chelating Activity - [MoA] (Mechanism of Action)
- Plant Proteins - [CS]
- Vegetable Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 63479 - Apex Energetics Inc.
- 63479-1409 - N09
- 63479-1409-1 - 30 mL in 1 BOTTLE, GLASS
- 63479-1409 - N09
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 63479-1409-1 identifies a specific commercial package of 30 ml in 1 bottle, glass of N09 Bacterotox, a human over the counter drug labeled by Apex Energetics Inc.. This solution/ drops is formulated for sublingual use and contains aconitum napellus; atropa belladonna; calcium sulfate anhydrous; calcium sulfide; calendula officinalis flowering top; echinacea angustifolia; ferrosoferric phosphate; garlic; goldenseal; lachesis muta venom; onion; silicon dioxide; thuja occidentalis leafy twig; virola sebifera resin 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 December 15, 1994. 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: 63479140901. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.