Renatone NDC 44911-0249

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0249Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0249Add 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
44911-0249-1	44911024901	30 mL in 1 BOTTLE, DROPPER (44911-0249-1)Marketed from Aug 27, 2015

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): Renatone
Generic name (nonproprietary): berberis vulgaris, solidago virgaurea, cantharis, arsenicum album, coccus cacti, lycopodium clavatum, phosphorus, senecio aureus
Active ingredients: Berberis vulgaris root bark — 3 [hp_X]/mLSolidago virgaurea flowering top — 3 [hp_X]/mLLytta vesicatoria — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLProtortonia cacti — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPackera aurea whole — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 27, 2015
Marketing end: Apr 13, 2027
Identifiers: Product ID 44911-0249_12492c1c-badc-446c-9039-dd7b701f64e0SPL ID 12492c1c-badc-446c-9039-dd7b701f64e0SPL set ID a1b88ba5-18e1-480b-8bd8-03bda85a7ef1UNII 1TH8Q20J0U, 5405K23S50, 3Q034RO3BT, S7V92P67HO, LZB7TFX1LT, C88X29Y479, 27YLU75U4W, 5WS1632J8WUPC 0363113700831

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

N444911024901 followed by a unit qualifier and the quantity

Package 44911-0249-01. 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 Oct 6, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve urine that is scanty, dark, and offensive, pain in the back, and sensation as if some urine remained after urinating.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)