apo-RHEUM NDC 59469-134

NDC codes

FDA NDC Directory

Product NDC (as listed)59469-134Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59469-0134Add 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
59469-134-10	59469013410	1 BOTTLE, GLASS in 1 BOX (59469-134-10) / 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): apo-RHEUM
Generic name (nonproprietary): arnica montana root, bryonia dioica root, colchicum autumnale bulb, solanum dulcamara top, pseudognaphalium obtusifolium, guaiacum officinale resin, and taraxacum officinale whole
Active ingredients: Arnica montana root — 12 [hp_X]/50mLBryonia dioica root — 4 [hp_X]/50mLColchicum autumnale bulb — 12 [hp_X]/50mLSolanum dulcamara top — 12 [hp_X]/50mLPseudognaphalium obtusifolium whole — 4 [hp_X]/50mLGuaiacum officinale resin — 6 [hp_X]/50mLTaraxacum officinale whole — 12 [hp_X]/50mL
Dosage form: Solution/ drops
Route: Oral
Labeler: PEKANA Naturheilmittel GmbH
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 11, 2008
Listing expires: Dec 31, 2026
Identifiers: Product ID 59469-134_0cab30b5-68eb-44ed-aaf1-a41f725a8d8eSPL ID 0cab30b5-68eb-44ed-aaf1-a41f725a8d8eSPL set ID e0e56d69-8c55-42c3-861b-27bc325b5bfdUNII MUE8Y11327, 53UB5FH7CX, 993QHL78E6, KPS1B1162N, 36XQ854NWW, N0K2Z502R6, 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

N459469013410 followed by a unit qualifier and the quantity

Package 59469-0134-10. 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 5, 2022.

Indications (excerpt from the label)

Indications For relief of minor joint pain. 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)