Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum Gel
NDC Package 57520-1502-4

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

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum gel is a drug for further processing. This formulation utilizes a gel delivery system. Marketed by Apotheca Company, this product is identified by NDC 57520-1502.

Identification & Billing

NDC Package Code
57520-1502-4
Package Description
2645 kg in 1 CONTAINER
Product Code
57520-1502
11-Digit Billing Format
57520150204

Clinical Specifications

Proprietary Name
Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum
Non-Proprietary Name
Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum
Substance Name
Achillea Millefolium Whole; Arnica Montana Whole; Atropa Belladonna; Bellis Perennis Whole; Calcium Fluoride; Calendula Officinalis Flowering Top; Comfrey Root; Ferrosoferric Phosphate; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum Whole; Oyster Shell Calcium Carbonate, Crude; Rhododendron Tomentosum Leafy Twig; Ruta Graveolens Flowering Top; Sodium Sulfate; Sulfuric Acid; Toxicodendron Pubescens Leaf
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Active Ingredient(s)

Regulatory & Marketing

Labeler Name
Apotheca Company
Product Type
Drug For Further Processing
Marketing Category
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date
12-22-2025
Listing Expiration
12-31-2027
Exclude Flag
N
Unfinished Product
Yes
Sample Package
N/A

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 57520-1502-4 identifies a specific commercial package of 2645 kg in 1 container of Calendula Officinalis, Hamamelis Virginiana, Arnica Montana, Hypericum Perforatum, Symphytum Officinale, Bellis Perennis, Ledum Palustre, Millefolium, Sulphuricum Acidum, Belladonna, Calcarea Fluorica, Ferrum Phosphoricum, Rhus Tox, Ruta Graveolens, Calcarea Carbonica, Natrum Sulphuricum (UNFINISHED drug), drug for further processing labeled by Apotheca Company. This gel is formulated for use and contains achillea millefolium whole; arnica montana whole; atropa belladonna; bellis perennis whole; calcium fluoride; calendula officinalis flowering top; comfrey root; ferrosoferric phosphate; hamamelis virginiana root bark/stem bark; hypericum perforatum whole; oyster shell calcium carbonate, crude; rhododendron tomentosum leafy twig; ruta graveolens flowering top; sodium sulfate; sulfuric acid; toxicodendron pubescens leaf 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 Apotheca Company on December 22, 2025. The current certification is valid through December 31, 2027.

How is this Apotheca Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 57520150204. 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)
57520-1502-4
11-Digit CMS (5-4-2)
57520-1502-04

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