Renal Drops 5024 (renal drops) NDC 63083-5024

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-5024Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-5024Add 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
63083-5024-2	63083502402	59 mL in 1 BOTTLE, DROPPER (63083-5024-2)Marketed from Aug 15, 1985

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): Renal Drops 5024Suffix: 5024
Generic name (nonproprietary): renal drops
Active ingredients: Rubia tinctorum root — 1 [hp_X]/59mLUrtica urens whole — 1 [hp_X]/59mLLycopodium clavatum spore — 2 [hp_X]/59mLSmilax ornata root — 3 [hp_X]/59mLBenzoic acid — 4 [hp_X]/59mLLithium carbonate — 4 [hp_X]/59mLBerberis vulgaris root bark — 5 [hp_X]/59mLProtortonia cacti — 5 [hp_X]/59mLSilver nitrate — 6 [hp_X]/59mLAtropine sulfate — 6 [hp_X]/59mLCitrullus colocynthis fruit pulp — 6 [hp_X]/59mLBeef kidney — 6 [hp_X]/59mLPetroselinum crispum root — 6 [hp_X]/59mLTaraxacum officinale — 6 [hp_X]/59mLCalcium hexafluorosilicate — 10 [hp_X]/59mLOyster shell calcium carbonate, Crude — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Ammonium Ion Binding Activity (Mechanism)Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers: Product ID 63083-5024_03049493-068f-4799-9c22-bf055de18e32SPL ID 03049493-068f-4799-9c22-bf055de18e32SPL set ID e598ae46-3b14-4dce-b7e0-abf159d102dbUNII 0SVP95L23G, IHN2NQ5OF9, C88X29Y479, 2H1576D5WG, 8SKN0B0MIM, 2BMD2GNA4V, 1TH8Q20J0U, LZB7TFX1LT, 95IT3W8JZE, 03J5ZE7KA5, 23H32AOH17, 5HOC10FSIC, 030FN29S9H, 39981FM375, 2NVP93XVQ3, 2E32821G6I
Pharmacologic class: Anticholinergic; Cholinergic Muscarinic Antagonist; Mood Stabilizer; 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

N463083502402 followed by a unit qualifier and the quantity

Package 63083-5024-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of minor nausea or vomiting, mild abdominal pain, changes in appetite, fatigue, disturbed sleep, or muscle cramps.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)