Virus Defense ANNAKARE NDC 71753-1258

NDC codes

FDA NDC Directory

Product NDC (as listed)71753-1258Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71753-1258Add 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
71753-1258-1	71753125801	30 mL in 1 BOTTLE, SPRAY (71753-1258-1)Marketed from Dec 2, 2022

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): Virus Defense ANNAKARE
Generic name (nonproprietary): aconitum napellus root, arsenic trioxide, baptisia tinctoria whole, bryonia alba root, echinacea angustifolia whole, eupatorium perfoliatum whole, gelsemium sempervirens whole, glycyrrhiza glabra, hydrastis canadensis whole, toxicodendron pubescens leaf
Active ingredients: Aconitum napellus root — 12 [hp_X]/30mLArsenic trioxide — 12 [hp_X]/30mLBaptisia tinctoria root — 12 [hp_X]/30mLBryonia alba root — 12 [hp_X]/30mLEchinacea angustifolia whole — 3 [hp_X]/30mLEupatorium perfoliatum whole — 12 [hp_X]/30mLGelsemium sempervirens whole — 12 [hp_X]/30mLGlycyrrhiza glabra — 3 [hp_X]/30mLHydrastis canadensis whole — 6 [hp_X]/30mLToxicodendron pubescens leaf — 12 [hp_X]/30mL
Dosage form: Spray
Route: Oral
Labeler: Ratis, LLC
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 2, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 71753-1258_40485cba-0bcd-598e-e063-6294a90ab71bSPL ID 40485cba-0bcd-598e-e063-6294a90ab71bSPL set ID 147f3bee-0fbc-472d-aade-90897550b836UNII KPD2N7348X, S7V92P67HO, 5EF0HWI5WU, T7J046YI2B, VB06AV5US8, 0LMC25OLZY, R0519OZO3K, 2788Z9758H, R763EBH88T, 6IO182RP7AUPC 0371753125815
Pharmacologic class: Non-Standardized Food Allergenic Extract; 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

N471753125801 followed by a unit qualifier and the quantity

Package 71753-1258-01. 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 Oct 3, 2025.

Full label on DailyMed (opens in a new tab)