Proaller NDC 59469-116

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-116Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0116Add 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
59469-116-10	59469011610	1 BOTTLE, GLASS in 1 BOX (59469-116-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Dec 11, 2008

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): Proaller
Generic name (nonproprietary): ailanthus altissima whole, okoubaka aubrevillei bark, euphrasia stricta, gratiola officinalis, juglans regia whole, smilax regelii root, and taraxacum officinale whole
Active ingredients: Ailanthus altissima whole — 4 [hp_X]/50mLOkoubaka aubrevillei bark — 3 [hp_X]/50mLEuphrasia stricta — 3 [hp_X]/50mLGratiola officinalis whole — 4 [hp_X]/50mLJuglans regia whole — 6 [hp_X]/50mLSmilax ornata root — 8 [hp_X]/50mLTaraxacum officinale whole — 12 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-116_78ed18a7-da36-4ead-be28-92693f46c272SPL ID 78ed18a7-da36-4ead-be28-92693f46c272SPL set ID 101ff372-e618-4c06-bad1-e2bfbc9e4349UNII 5G78C6GB5E, MK2074187Z, C9642I91WL, BDD9991A36, 87EJ76IO83, 2H1576D5WG, 7C42E2D7B0

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

N459469011610 followed by a unit qualifier and the quantity

Package 59469-0116-10. 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 Dec 19, 2022.

Indications (excerpt from the label)

Indications For temporary relief of allergies and hay fever symptoms. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)