Renapath NDC 64578-0103

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0103Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0103Add 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
64578-0103-1	64578010301	59.1 mL in 1 BOTTLE, DROPPER (64578-0103-1)Marketed from Jul 13, 2017

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): Renapath
Generic name (nonproprietary): benzoicum acidum, berberis vulgaris, bryonia, dna, eupatorium purpureum, glandula suprarenalis suis, hydrangea arborescens, hypothalamus, mercurius corrosivus, pancreas suis, pareira brava, petroselinum sativum, pituitarum posterium, rubia tinctorum, sarsaparilla, solidago virgaurea, thyroidinum (bovine), uva-ursi
Active ingredients: Chondrodendron tomentosum root — 10 [hp_X]/mLPetroselinum crispum — 4 [hp_X]/mLSus scrofa pituitary gland — 12 [hp_X]/mLRubia tinctorum root — 6 [hp_X]/mLSarsaparilla — 4 [hp_X]/mLSolidago virgaurea flowering top — 4 [hp_X]/mLThyroid, Bovine — 9 [hp_X]/mLArctostaphylos uva-ursi leaf — 4 [hp_X]/mLBenzoic acid — 10 [hp_X]/mLBerberis vulgaris root bark — 4 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLHerring sperm DNA — 12 [hp_X]/mLEutrochium purpureum root — 12 [hp_X]/mLSus scrofa adrenal gland — 9 [hp_X]/mLHydrangea arborescens root — 4 [hp_X]/mLBos taurus hypothalamus — 12 [hp_X]/mLMercuric chloride — 12 [hp_X]/mLSus scrofa pancreas — 9 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 6, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Ammonium Ion Binding Activity (Mechanism)
Identifiers: Product ID 64578-0103_58ca2513-a466-52d6-e063-6394a90a634cSPL ID 58ca2513-a466-52d6-e063-6394a90a634cSPL set ID 1a37b994-9470-4266-a4e1-008538ea0edfUNII 395A3P448Z, 1WZA4Y92EX, L0PFEMQ1DT, 0SVP95L23G, 2H1576D5WG, 5405K23S50, MN18OTN73W, 3M5V3D1X36, 8SKN0B0MIM, 1TH8Q20J0U, T7J046YI2B, 51FI676N6F, 0VYG5PVN5Q, 398IYQ16YV, SFK828Q2DE, S6G2NLH4Y7, 53GH7MZT1R, 9Y3J3362RY
Pharmacologic class: Nitrogen Binding Agent

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

N464578010301 followed by a unit qualifier and the quantity

Package 64578-0103-01. 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 Aug 11, 2026.

Indications (excerpt from the label)

Uses Temporary relief of copious or diminished urination, occasional swelling in extremities.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)