Renapar NDC 44911-0641

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0641Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0641Add 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
44911-0641-1	44911064101	30 mL in 1 BOTTLE, DROPPER (44911-0641-1)Marketed from Jun 7, 2021

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): Renapar
Generic name (nonproprietary): pareira brava, petroselinum sativum, sarsaparilla (smilax regelii), kidney (suis), bryonia (alba), mercurius corrosivus, rubia tinctorum, solidago virgaurea, triticum repens
Active ingredients: Chondrodendron tomentosum root — 8 [hp_X]/mLPetroselinum crispum whole — 3 [hp_X]/mLSmilax ornata root — 3 [hp_X]/mLPork kidney — 6 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLRubia tinctorum root — 12 [hp_X]/mLSolidago virgaurea flowering top — 12 [hp_X]/mLElymus repens root — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 7, 2021
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0641_c7b9e887-b6eb-4a7b-9db3-0ec22baf4c8bSPL ID c7b9e887-b6eb-4a7b-9db3-0ec22baf4c8bSPL set ID 0515331b-c3d2-4426-ac28-8ef6018352a5UNII 395A3P448Z, 1WZA4Y92EX, 2H1576D5WG, X7BCI5P86H, T7J046YI2B, 53GH7MZT1R, 0SVP95L23G, 5405K23S50, 3IXW0F6P8WUPC 0363113700978

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

N444911064101 followed by a unit qualifier and the quantity

Package 44911-0641-01. 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 Dec 1, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve sudden desire to urinate, urination difficult and scanty, and frequent urging on urination.** **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)