C04 Solution/ Drops
NDC Package 63479-0304-1

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

Package Information

C04 (actaea spicata, ammonium benzoicum, arnica montana, bellis perennis, berberis vulgaris, bryonia, chelidonium majus, chininum sulphuricum, dulcamara lignosa whole, echinacea purpurea, formica rufa, fraxinus excelsior leaf, lacticum acidum, ledum palustre, pulsatilla vulgaris, rhododendron chrysanthum, rhus toxicodendron, ruta graveolens, sarcolacticum acidum, symphytum officinale, uricum acidum) solution/ dropses is adults & children ages 12 years and over: Take 8 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 63479-0304.

Identification & Billing

NDC Package Code
63479-0304-1
Package Description
30 mL in 1 BOTTLE, GLASS
Product Code
63479-0304
11-Digit Billing Format
63479030401

Clinical Specifications

Proprietary Name
C04 Arthro Muscotox
Non-Proprietary Name
Actaea Spicata, Ammonium Benzoicum, Arnica Montana, Bellis Perennis, Berberis Vulgaris, Bryonia, Chelidonium Majus, Chininum Sulphuricum, Dulcamara Lignosa Whole, Echinacea Purpurea, Formica Rufa, Fraxinus Excelsior Leaf, Lacticum Acidum, Ledum Palustre, Pulsatilla Vulgaris, Rhododendron Chrysanthum, Rhus Toxicodendron, Ruta Graveolens, Sarcolacticum Acidum, Symphytum Officinale, Uricum Acidum
Substance Name
Actaea Spicata Root; Ammonium Benzoate; Arnica Montana; Bellis Perennis; Berberis Vulgaris Root Bark; Bryonia Alba Root; Chelidonium Majus; Comfrey Root; Echinacea Purpurea; Formica Rufa; Fraxinus Excelsior Leaf; Lactic Acid, Dl-; Lactic Acid, L-; Pulsatilla Vulgaris Whole; Quinine Sulfate; Rhododendron Aureum Leaf; Rhododendron Tomentosum Leafy Twig; Ruta Graveolens Flowering Top; Solanum Dulcamara Whole; Toxicodendron Pubescens Leaf; Uric Acid
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
Antimalarial - [EPC] (Established Pharmacologic Class)
Usage Information
Adults & children ages 12 years and over: Take 8 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
12-15-1994
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 63479-0304-1 identifies a specific commercial package of 30 ml in 1 bottle, glass of C04 Arthro Muscotox, a human over the counter drug labeled by Apex Energetics Inc.. This solution/ drops is formulated for sublingual use and contains actaea spicata root; ammonium benzoate; arnica montana; bellis perennis; berberis vulgaris root bark; bryonia alba root; chelidonium majus; comfrey root; echinacea purpurea; formica rufa; fraxinus excelsior leaf; lactic acid, dl-; lactic acid, l-; pulsatilla vulgaris whole; quinine sulfate; rhododendron aureum leaf; rhododendron tomentosum leafy twig; ruta graveolens flowering top; solanum dulcamara whole; toxicodendron pubescens leaf; uric acid 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: 63479030401. 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)
63479-0304-1
11-Digit CMS (5-4-2)
63479-0304-01

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