Allergiemittel NDC 53499-3590

NDC codes

FDA NDC Directory

Product NDC (as listed)53499-3590Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53499-3590Add 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
53499-3590-1	53499359001	4 BLISTER PACK in 1 CARTON (53499-3590-1) / 10 TABLET in 1 BLISTER PACKMarketed from Apr 28, 2020

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): Allergiemittel
Generic name (nonproprietary): cardiospermum halicacabum flowering top, galphimia glauca flowering top, luffa operculata fruit
Active ingredients: Cardiospermum halicacabum flowering top — 3 [hp_X]/1Galphimia glauca flowering top — 3 [hp_X]/1Luffa operculata fruit — 5 [hp_X]/1
Dosage form: Tablet
Route: Sublingual
Labeler: Schwabe North America, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 28, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 53499-3590_e2937205-cb32-4342-bb47-77286a75fee5SPL ID e2937205-cb32-4342-bb47-77286a75fee5SPL set ID 8aa3cd06-5a3a-4a16-9784-fbac3fc9c97bUNII MZP2508BRR, 93PH5Q8M7E, C4MO6809HUUPC 0308078125909

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N453499359001 followed by a unit qualifier and the quantity

Package 53499-3590-01. 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 Nov 25, 2025.

Indications (excerpt from the label)

Indications and Usage Temporarily relieves minor allergic symptoms: sneezing; runny, stuffy, itchy nose, red, itchy, watery eyes, scratchy throat.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)