Coffea cruda (arabica coffee bean) NDC 0220-1444

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-1444Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-1444Add 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
0220-1444-41	00220144441	30 [hp_C] in 1 TUBE (0220-1444-41)Marketed from Mar 3, 1983
0220-1444-43	00220144443	3 TUBE in 1 BOX (0220-1444-43) / 30 [hp_C] in 1 TUBEMarketed from Sep 1, 2020

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): Coffea cruda
Generic name (nonproprietary): arabica coffee bean
Active ingredients: Arabica coffee bean — 30 [hp_C]/30[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
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 0220-1444_42dd7102-2dfe-fbf2-e063-6394a90afa8aSPL ID 42dd7102-2dfe-fbf2-e063-6394a90afa8aSPL set ID 853d26eb-e3b8-4afa-e053-2a91aa0a85c3UNII 3SW678MX72
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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

N400220144441 followed by a unit qualifier and the quantity

Package 00220-1444-41. 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 Nov 5, 2025.

Indications (excerpt from the label)

Uses* temporarily relieves occasional sleeplessness or restless sleep due to: mental hyperactivity racing thoughts obsessive thoughts worries or concerns helps to reduce difficulty falling asleep

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)