Genexa Allergy Care Tablet, Chewable
NDC Package 69676-0052-3

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Genexa Allergy Care (allium cepa, ambrosia artemisiifolia, arundo mauritanica, dulcamara, euphrasia officinalis, nux vomica, pulsatilla, ranunculus bulbosus, sabadilla, sinapis nigra, sticta pulmonaria, wyethia helenoides) tablets is uses*addresses symptoms associated with hay fever or other upper respiratory allergies, such as:irritated eyessinus pressurenasal congestionrunny nosesneezingitchy throat & nose. This formulation utilizes a tablet, chewable delivery system. Marketed by Genexa Inc., this product is identified by NDC 69676-0052.

Identification & Billing

NDC Package Code
69676-0052-3
Package Description
2 TABLET, CHEWABLE in 1 POUCH
Product Code
11-Digit Billing Format
69676005203

Clinical Specifications

Proprietary Name
Genexa Allergy Care
Non-Proprietary Name
Allium Cepa, Ambrosia Artemisiifolia, Arundo Mauritanica, Dulcamara, Euphrasia Officinalis, Nux Vomica, Pulsatilla, Ranunculus Bulbosus, Sabadilla, Sinapis Nigra, Sticta Pulmonaria, Wyethia Helenoides
Substance Name
Allium Cepa Whole; Ambrosia Artemisiifolia; Arundo Pliniana Root; Black Mustard Seed; Euphrasia Stricta; Lobaria Pulmonaria; Pulsatilla Pratensis; Ranunculus Bulbosus Whole; Schoenocaulon Officinale Seed; Solanum Dulcamara Top; Strychnos Nux-vomica Seed; Wyethia Helenioides Root
Dosage Form
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Uses*addresses symptoms associated with hay fever or other upper respiratory allergies, such as:irritated eyessinus pressurenasal congestionrunny nosesneezingitchy throat & nose

Regulatory & Marketing

Labeler Name
Genexa Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
12-01-2020
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
Yes

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (69676-0052). Click a package code to view its specific billing and regulatory data.

1 BOTTLE, PLASTIC in 1 CARTON / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

* 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 69676-0052-3 identifies a specific commercial package of 2 tablet, chewable in 1 pouch of Genexa Allergy Care, a human over the counter drug labeled by Genexa Inc.. This tablet, chewable is formulated for oral use and contains allium cepa whole; ambrosia artemisiifolia; arundo pliniana root; black mustard seed; euphrasia stricta; lobaria pulmonaria; pulsatilla pratensis; ranunculus bulbosus whole; schoenocaulon officinale seed; solanum dulcamara top; strychnos nux-vomica seed; wyethia helenioides root 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 Genexa Inc. on December 01, 2020. The current certification is valid through December 31, 2027.

How is this Genexa Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69676005203. 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)
69676-0052-3
11-Digit CMS (5-4-2)
69676-0052-03

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