Proteinuria Drops 2053 (proteinuria drops) NDC 63083-2053

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2053Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2053Add 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
63083-2053-2	63083205302	59 mL in 1 BOTTLE, DROPPER (63083-2053-2)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): Proteinuria Drops 2053Suffix: 2053
Generic name (nonproprietary): proteinuria drops
Active ingredients: Berberis vulgaris root bark — 6 [hp_X]/59mLEquisetum arvense top — 6 [hp_X]/59mLBeef kidney — 6 [hp_X]/59mLRhododendron tomentosum leafy twig — 12 [hp_X]/59mLPhosphorus — 12 [hp_X]/59mLAlbumin human — 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: Increased Intravascular Volume (Physiologic effect)Increased Oncotic Pressure (Physiologic effect)Osmotic Activity (Mechanism)Serum Albumin (Chemical/Ingredient)
Identifiers: Product ID 63083-2053_9405275a-a05e-4f42-a823-7e13173c49d9SPL ID 9405275a-a05e-4f42-a823-7e13173c49d9SPL set ID 1bf80282-8283-4835-acd4-fbdb47788c67UNII 1TH8Q20J0U, 1DP6Y6B65Z, 5HOC10FSIC, 877L01IZ0P, 27YLU75U4W, ZIF514RVZR
Pharmacologic class: Human Serum Albumin

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

N463083205302 followed by a unit qualifier and the quantity

Package 63083-2053-02. 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 mild pain in the back or abdomen, bloating, foaming urine, or swelling of small joints.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)