Renelix Solution/ Drops
NDC Package 59469-315-10
Package Information
Renelix (benzoic acid, nitric acid, apis mellifera, berberis vulgaris root bark, colchicum autumnale bulb, protortonia cacti, solidago virgaurea flowering top, and capsella bursa-pastoris top) solution/ dropses is a medication used as Helps cleanse and detoxify the body. This formulation utilizes a solution/ drops delivery system. Marketed by Pekana Naturheilmittel Gmbh, this product is identified by NDC 59469-315.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Ammonium Ion Binding Activity - [MoA] (Mechanism of Action)
- Bee Venoms - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Nitrogen Binding Agent - [EPC] (Established Pharmacologic Class)
- Standardized Insect Venom Allergenic Extract - [EPC] (Established Pharmacologic Class)
Regulatory & Marketing
Hierarchy Structure
- 59469 - Pekana Naturheilmittel Gmbh
- 59469-315 - Renelix
- 59469-315-10 - 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
- 59469-315 - Renelix
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (59469-315). Click a package code to view its specific billing and regulatory data.
* 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 59469-315-10 identifies a specific commercial package of 1 bottle, glass in 1 box / 50 ml in 1 bottle, glass of Renelix, a human over the counter drug labeled by Pekana Naturheilmittel Gmbh. This solution/ drops is formulated for oral use and contains apis mellifera; benzoic acid; berberis vulgaris root bark; capsella bursa-pastoris top; colchicum autumnale bulb; nitric acid; protortonia cacti; solidago virgaurea flowering top 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 Gmbh on June 24, 2019. The current certification is valid through December 31, 2026.
How is this Pekana Naturheilmittel Gmbh product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 59469031510. 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 Product segment to maintain the 5-4-2 structure.