Allercetin NDC 64471-196

NDC codes

FDA NDC Directory

Product NDC (as listed)64471-196Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64471-0196Add 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
64471-196-48	64471019648	7200 mg in 1 BLISTER PACK (64471-196-48)Marketed from Sep 5, 2014

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Allercetin
Generic name (nonproprietary): euphrasia officinalis, kali iodatum, sabadilla, sticta pulmonaria, histaminum hydrochloricum, quercetin, succinicum acidum, ambrosia artemisiaefolia
Active ingredients: Euphrasia stricta — 6 [hp_X]/mgPotassium iodide — 6 [hp_X]/mgSchoenocaulon officinale seed — 6 [hp_X]/mgLobaria pulmonaria — 6 [hp_X]/mgHistamine dihydrochloride — 12 [hp_X]/mgQuercetin — 12 [hp_X]/mgSuccinic acid — 12 [hp_X]/mgAmbrosia artemisiifolia whole — 30 [hp_X]/mg
Dosage form: Tablet, Chewable
Route: Oral
Labeler: Source Naturals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 5, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 64471-196_85e768b9-7a6c-4a8f-9e15-9523963e505cSPL ID 85e768b9-7a6c-4a8f-9e15-9523963e505cSPL set ID a06106dd-4ca6-4c7f-99b3-b8e464bf59bbUNII C9642I91WL, 1C4QK22F9J, 6NAF1689IO, D1YM0P5Z2T, 3POA0Q644U, 9IKM0I5T1E, AB6MNQ6J6L, 9W34L2CQ9A

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

N464471019648 followed by a unit qualifier and the quantity

Package 64471-0196-48. 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 31, 2024.

Indications (excerpt from the label)

USES: *temporary relieves these symptoms due to hay fever or other upper respiratory allergies: • sneezing • runny nose • itchy and watery eyes • sinus congestion and headache. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)