Cataract Drops 2085 (cataract drops) NDC 63083-2085

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2085Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2085Add 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
63083-2085-2	63083208502	59 mL in 1 BOTTLE, DROPPER (63083-2085-2)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): Cataract Drops 2085Suffix: 2085
Generic name (nonproprietary): cataract drops
Active ingredients: Euphrasia stricta — 1 [hp_X]/59mLBilberry — 1 [hp_X]/59mLCalcium fluoride — 6 [hp_X]/59mLJacobaea maritima leaf — 6 [hp_X]/59mLBos taurus eye — 6 [hp_X]/59mLZinc — 6 [hp_X]/59mLPhosphorus — 8 [hp_X]/59mLGermanium — 10 [hp_X]/59mLCausticum — 12 [hp_X]/59mLSilicon dioxide — 12 [hp_X]/59mLSodium chloride — 30 [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
Identifiers: Product ID 63083-2085_660a2396-2524-47f8-a1dc-fed0c231b9ebSPL ID 660a2396-2524-47f8-a1dc-fed0c231b9ebSPL set ID 6040a096-ccdb-4e1e-a242-be29c3127f27UNII C9642I91WL, 9P2U39H18W, O3B55K4YKI, 6069DS9S3U, VTW461N43P, J41CSQ7QDS, 27YLU75U4W, 00072J7XWS, DD5FO1WKFU, ETJ7Z6XBU4, 451W47IQ8X

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

N463083208502 followed by a unit qualifier and the quantity

Package 63083-2085-02. 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 occasional clouded, blurred, or dim vision.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)