Genexa Allergy Care NDC 69676-0052

NDC codes

FDA NDC Directory

Product NDC (as listed)69676-0052Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69676-0052Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
69676-0052-1	69676005201	1 BOTTLE, PLASTIC in 1 CARTON (69676-0052-1) / 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTICMarketed from Dec 1, 2020
69676-0052-3	69676005203	2 TABLET, CHEWABLE in 1 POUCH (69676-0052-3)Marketed from Dec 8, 2022 · Sample package

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Genexa Allergy Care
Generic name (nonproprietary): allium cepa, ambrosia artemisiifolia, arundo mauritanica, dulcamara, euphrasia officinalis, nux vomica, pulsatilla, ranunculus bulbosus, sabadilla, sinapis nigra, sticta pulmonaria, wyethia helenoides
Active ingredients: Ambrosia artemisiifolia — 12 [hp_X]/1Strychnos nux-vomica seed — 12 [hp_X]/1Black mustard seed — 12 [hp_X]/1Lobaria pulmonaria — 12 [hp_X]/1Arundo pliniana root — 12 [hp_X]/1Ranunculus bulbosus whole — 12 [hp_X]/1Pulsatilla pratensis — 12 [hp_X]/1Schoenocaulon officinale seed — 12 [hp_X]/1Solanum dulcamara top — 12 [hp_X]/1Euphrasia stricta — 12 [hp_X]/1Wyethia helenioides root — 12 [hp_X]/1Allium cepa whole — 12 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: Genexa Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 69676-0052_59af45df-ac36-9901-e063-6294a90a71aaSPL ID 59af45df-ac36-9901-e063-6294a90a71aaSPL set ID b5fddd8f-a380-6e88-e053-2a95a90a6b89UNII 9W34L2CQ9A, 269XH13919, 8LTY55LQ8D, D1YM0P5Z2T, ZXE7LB03WC, AEQ8NXJ0MB, 8E272251DI, 6NAF1689IO, KPS1B1162N, C9642I91WL, J10PD1AQ0N, 8P2VLG2456UPC 0857630006052
Pharmacologic class: Non-Standardized Plant Allergenic Extract

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N469676005201 followed by a unit qualifier and the quantity

Package 69676-0052-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Aug 22, 2026.

Indications (excerpt from the label)

Uses* addresses symptoms associated with hay fever or other upper respiratory allergies, such as: sneezing runny nose itchy, watery eyes nasal congestion itchy nose & throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)