Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Renapar NDC 44911-0641
Chondrodendron tomentosum root 8 [hp_X]/mL + 8 more ingredients · Liquid · Oral · Energique, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 44911-0641-1 | 4491106410144911064101 | 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.NDC labeler code 44911
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- 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
N444911064101followed by a unit qualifier and the quantityPackage 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 .
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.
About NDC 44911-0641
- What is NDC 44911-0641?
- 44911-0641 is the product NDC for Renapar, Chondrodendron tomentosum root 8 [hp_X]/mL + 8 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Renapar (Pareira Brava, Petroselinum Sativum, Sarsaparilla (Smilax Regelii), Kidney (Suis), Bryonia (Alba), Mercurius Corrosivus, Rubia Tinctorum, Solidago Virgaurea, Triticum Repens).
- What is the active ingredient?
- Chondrodendron tomentosum root, Petroselinum crispum whole, Smilax ornata root, Pork kidney, Bryonia alba root, Mercuric chloride, Rubia tinctorum root, Solidago virgaurea flowering top, Elymus repens root.
- Who is the labeler?
- Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Renapar?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.