Euphrasia officinalis (euphrasia stricta) NDC 0220-1989

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-1989Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-1989Add 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
0220-1989-41	00220198941	6 [hp_C] in 1 TUBE (0220-1989-41)Marketed from Mar 3, 1983
0220-1989-43	00220198943	3 TUBE in 1 CARTON (0220-1989-43) / 6 [hp_C] in 1 TUBE (0220-1989-41)Marketed from Jun 4, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Euphrasia officinalis
Generic name (nonproprietary): euphrasia stricta
Active ingredients: Euphrasia stricta — 6 [hp_C]/6[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-1989_1a14e2b8-73e9-f02f-e063-6294a90a2c87SPL ID 1a14e2b8-73e9-f02f-e063-6294a90a2c87SPL set ID 85904faf-92c5-1da7-e053-2a91aa0a66d8UNII C9642I91WL

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

N400220198941 followed by a unit qualifier and the quantity

Package 00220-1989-41. 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 Jun 4, 2024.

Indications (excerpt from the label)

Allergy Eye Relief Uses* temporarily relieves minor eye allergy symptoms such as: itching irritation burning watering redness Tube Uses* Relieves abundant and irritating eye discharge *

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)