Proscenat NDC 59469-314

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-314Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0314Add 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
59469-314-10	59469031410	1 BOTTLE, GLASS in 1 BOX (59469-314-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019

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): Proscenat
Generic name (nonproprietary): sulfuric acid, lytta vesicatoria, conium maculatum flowering top, selenium, delphinium staphisagria seed, nasturtium officinale whole, and ononis spinosa whole
Active ingredients: Sulfuric acid — 6 [hp_X]/50mLLytta vesicatoria — 4 [hp_X]/50mLConium maculatum flowering top — 4 [hp_X]/50mLSelenium — 8 [hp_X]/50mLDelphinium staphisagria seed — 6 [hp_X]/50mLNasturtium officinale whole — 1852 mg/50mLOnonis spinosa whole — 2564 mg/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 24, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-314_2d2d5f9d-97c8-424f-83e1-d2f7dddee82dSPL ID 2d2d5f9d-97c8-424f-83e1-d2f7dddee82dSPL set ID 1fe525a2-7ff6-4704-ab47-08552eb5ba4aUNII O40UQP6WCF, 3Q034RO3BT, Q28R5GF371, H6241UJ22B, 00543AP1JV, P7LJ54BP7G, RP8496915M

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

N459469031410 followed by a unit qualifier and the quantity

Package 59469-0314-10. 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 Jan 11, 2023.

Indications (excerpt from the label)

Indications For relief of minor painful urination. 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)