EyeClear Pro NDC 68703-387

NDC codes

FDA NDC Directory

Product NDC (as listed)68703-387Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68703-0387Add 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
68703-387-02	68703038702	59 mL in 1 BOTTLE, GLASS (68703-387-02)Marketed from Mar 13, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): EyeClear Pro
Generic name (nonproprietary): calc carb, calc fluor, causticum, cineraria, euphrasia, naphthalinum, nat mur, phos, quassia, silicea
Active ingredients: Naphthalene — 30 [hp_X]/59mLCausticum — 30 [hp_X]/59mLCalcium fluoride — 30 [hp_X]/59mLSenecio vulgaris — 30 [hp_X]/59mLOyster shell calcium carbonate, Crude — 30 [hp_X]/59mLSilicon dioxide — 30 [hp_X]/59mLSodium chloride — 30 [hp_X]/59mLPhosphorus — 30 [hp_X]/59mLEuphrasia stricta — 30 [hp_X]/59mLQuassia amara wood — 30 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Silver Star Brands
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 13, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 68703-387_f4d4943b-cb79-aa71-e053-2a95a90ac638SPL ID f4d4943b-cb79-aa71-e053-2a95a90ac638SPL set ID f4d4943b-cb78-aa71-e053-2a95a90ac638UNII 2166IN72UN, DD5FO1WKFU, O3B55K4YKI, W6MU8IYV12, 2E32821G6I, ETJ7Z6XBU4, 451W47IQ8X, 27YLU75U4W, C9642I91WL, S5249Q85HW

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

N468703038702 followed by a unit qualifier and the quantity

Package 68703-0387-02. 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 Feb 16, 2023.

Indications (excerpt from the label)

Uses* Uses*: For temporary relief of symptoms of common eye irritations: mineral accumulations, tearing, light sensitivity, eye fatigue, redness, itching. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)