Glautarakt Solution/ Drops
NDC Package 59469-131-10
Package Information
Glautarakt (gold trichloride, solanum dulcamara top, euphrasia stricta, nitroglycerin, hedera helix flowering twig, ruta graveolens flowering top, tobacco leaf, and cynara scolymus whole) solution/ dropses is a medication used as Supports proper eye function. This formulation utilizes a solution/ drops delivery system. Marketed by Pekana Naturheilmittel Gmbh, this product is identified by NDC 59469-131.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Nitrate Vasodilator - [EPC] (Established Pharmacologic Class)
- Nitrates - [CS]
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Vasodilation - [PE] (Physiologic Effect)
Regulatory & Marketing
Hierarchy Structure
- 59469 - Pekana Naturheilmittel Gmbh
- 59469-131 - Glautarakt
- 59469-131-10 - 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
- 59469-131 - Glautarakt
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 59469-131-10 identifies a specific commercial package of 1 bottle, glass in 1 box / 50 ml in 1 bottle, glass of Glautarakt, a human over the counter drug labeled by Pekana Naturheilmittel Gmbh. This solution/ drops is formulated for oral use and contains cynara scolymus whole; euphrasia stricta; gold trichloride; hedera helix flowering twig; nitroglycerin; ruta graveolens flowering top; solanum dulcamara top; tobacco 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 Pekana Naturheilmittel Gmbh on December 11, 2008. 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: 59469013110. 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.