Glucorekt Solution/ Drops
NDC Package 59469-308-10
Package Information
Glucorekt (lactic acid, dl-, sulfuric acid, onion, chionanthus virginicus bark, phosphorus, zinc sulfate heptahydrate, corn silk, and syzygium cumini fruit) solution/ dropses is a medication used as For support of digestive processes. This formulation utilizes a solution/ drops delivery system. Marketed by Pekana Naturheilmittel Gmbh, this product is identified by NDC 59469-308.
Identification & Billing
Clinical Specifications
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
- Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Vegetable Proteins - [CS]
Regulatory & Marketing
Hierarchy Structure
- 59469 - Pekana Naturheilmittel Gmbh
- 59469-308 - Glucorekt
- 59469-308-10 - 1 BOTTLE, GLASS in 1 BOX / 50 mL in 1 BOTTLE, GLASS
- 59469-308 - Glucorekt
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 59469-308-10 identifies a specific commercial package of 1 bottle, glass in 1 box / 50 ml in 1 bottle, glass of Glucorekt, a human over the counter drug labeled by Pekana Naturheilmittel Gmbh. This solution/ drops is formulated for oral use and contains chionanthus virginicus root bark; corn silk; lactic acid, dl-; onion; phosphorus; sulfuric acid; syzygium cumini fruit; zinc sulfate heptahydrate 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: 59469030810. 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.