Occuloplex I NDC 43857-0600

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0600Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0600Add 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
43857-0600-1	43857060001	30 mL in 1 BOTTLE, DROPPER (43857-0600-1)Marketed from Jun 15, 2021

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): Occuloplex ISuffix: I
Generic name (nonproprietary): euphrasia officinalis, ginkgo biloba, taraxacum officinale, hydrastis canadensis, glutathione, ubidecarenonum, zincum gluconicum, citrus bioflavonoids, eye (suis), ammonium muriaticum, calcarea fluorica, causticum, conium maculatum, cyanocobalamin, germanium sesquioxide, magnesia carbonica, selenium dioxide, silicea, beta carotene
Active ingredients: Euphrasia stricta — 3 [hp_X]/mLGinkgo — 3 [hp_X]/mLTaraxacum officinale — 3 [hp_X]/mLGoldenseal — 5 [hp_X]/mLGlutathione — 6 [hp_X]/mLUbidecarenone — 6 [hp_X]/mLZinc gluconate — 6 [hp_X]/mLCitrus bioflavonoids — 8 [hp_X]/mLSus scrofa eye — 8 [hp_X]/mLAmmonium chloride — 12 [hp_X]/mLCalcium fluoride — 12 [hp_X]/mLCausticum — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLCyanocobalamin — 12 [hp_X]/mLGermanium sesquioxide — 12 [hp_X]/mLMagnesium carbonate — 12 [hp_X]/mLSelenium dioxide — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLBeta carotene — 9 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 15, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Decreased Copper Ion Absorption (Physiologic effect)Vitamin B 12 (Chemical structure)
Identifiers: Product ID 43857-0600_32c14ba1-b46d-4714-9e7b-06e64c79a8daSPL ID 32c14ba1-b46d-4714-9e7b-06e64c79a8daSPL set ID c2c9b577-4f75-4ddc-815f-46c3bb9b46d2UNII C9642I91WL, 19FUJ2C58T, 39981FM375, ZW3Z11D0JV, GAN16C9B8O, EJ27X76M46, U6WSN5SQ1Z, BD70459I50, X3AOK514E6, 01Q9PC255D, O3B55K4YKI, DD5FO1WKFU, Q28R5GF371, P6YC3EG204, 96WE91N25T, 0E53J927NA, 9N3UK29E57, ETJ7Z6XBU4, 01YAE03M7J
Pharmacologic class: Copper Absorption Inhibitor; Vitamin B12

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

N443857060001 followed by a unit qualifier and the quantity

Package 43857-0600-01. 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 May 8, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of minor inflammation, burning & swelling of the eyelids.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)