Opsonat NDC 59469-313

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-313Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0313Add 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
59469-313-10	59469031310	1 BOTTLE, GLASS in 1 BOX (59469-313-10) / 50 mL in 1 BOTTLE, GLASSMarketed from Jun 24, 2019
59469-313-40	59469031340	1 BOTTLE, GLASS in 1 BOX (59469-313-40) / 100 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): Opsonat
Generic name (nonproprietary): silver nitrate, sulfuric acid, bellis perennis, lytta vesicatoria, gratiola officinalis, goldenseal, lachesis muta venom, and glechoma hederacea flowering top
Active ingredients: Silver nitrate — 6 [hp_X]/100mLSulfuric acid — 6 [hp_X]/100mLBellis perennis whole — 1 [hp_X]/100mLLytta vesicatoria — 4 [hp_X]/100mLGratiola officinalis whole — 4 [hp_X]/100mLGoldenseal — 5 [hp_X]/100mLLachesis muta venom — 8 [hp_X]/100mLGlechoma hederacea flowering top — 1602 mg/100mL
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 59469-313_78966d8c-4e59-42a5-b818-a4f191e94ae0SPL ID 78966d8c-4e59-42a5-b818-a4f191e94ae0SPL set ID 506f8227-207c-462c-a71c-5f8f00b4f8deUNII 95IT3W8JZE, O40UQP6WCF, 2HU33I03UY, 3Q034RO3BT, BDD9991A36, ZW3Z11D0JV, VSW71SS07I, 2458J91U39

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

N459469031310 followed by a unit qualifier and the quantity

Package 59469-0313-10. 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 mucous membrane inflammation, such as the mouth. 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)