Proaller Solution/ Drops
NDC Package 59469-116-10

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

Package Information

Proaller (ailanthus altissima whole, okoubaka aubrevillei bark, euphrasia stricta, gratiola officinalis, juglans regia whole, smilax regelii root, and taraxacum officinale whole) solution/ dropses is a medication used as For temporary relief of allergies and hay fever. This formulation utilizes a solution/ drops delivery system. Marketed by Pekana Naturheilmittel, this product is identified by NDC 59469-116.

Identification & Billing

NDC Package Code
59469-116-10
Package Description
1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
Product Code
59469-116
11-Digit Billing Format
59469011610

Clinical Specifications

Proprietary Name
Proaller
Non-Proprietary Name
Ailanthus Altissima Whole, Okoubaka Aubrevillei Bark, Euphrasia Stricta, Gratiola Officinalis, Juglans Regia Whole, Smilax Regelii Root, And Taraxacum Officinale Whole
Substance Name
Ailanthus Altissima Whole; Euphrasia Stricta; Gratiola Officinalis Whole; Juglans Regia Whole; Okoubaka Aubrevillei Bark; Smilax Ornata Root; Taraxacum Officinale Whole
Dosage Form
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
This product is used as For temporary relief of allergies and hay fever. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Regulatory & Marketing

Labeler Name
Pekana Naturheilmittel
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
12-11-2008
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 59469-116-10 identifies a specific commercial package of 1 bottle, glass in 1 box / 50 ml in 1 bottle, glass of Proaller, a human over the counter drug labeled by Pekana Naturheilmittel. This solution/ drops is formulated for oral use and contains ailanthus altissima whole; euphrasia stricta; gratiola officinalis whole; juglans regia whole; okoubaka aubrevillei bark; smilax ornata root; taraxacum officinale whole 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 Pekana Naturheilmittel on December 11, 2008. The current certification is valid through December 31, 2026.

How is this Pekana Naturheilmittel product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59469011610. 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 (5-3-2)
59469-116-10
11-Digit CMS (5-4-2)
59469-0116-10

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