SinusCalm NDC 0220-9347

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-9347Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-9347Add 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
0220-9347-42	00220934742	1 TUBE in 1 BOX (0220-9347-42) / 80 PELLET in 1 TUBE (0220-9347-41)Marketed from Dec 1, 2019

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): SinusCalm
Generic name (nonproprietary): atropa belladonna, sanguinaria canadensis root, spigelia anthelmia
Active ingredients: Sanguinaria canadensis root — 3 [hp_C]/1Atropa belladonna — 3 [hp_C]/1Spigelia anthelmia — 3 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Boiron
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 1, 2019
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-9347_08f2e848-c96f-4947-e063-6394a90a7310SPL ID 08f2e848-c96f-4947-e063-6394a90a7310SPL set ID 95872748-6d70-5c80-e053-2995a90a570cUNII N9288CD508, WQZ3G9PF0H, WYT05213GE

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

N400220934742 followed by a unit qualifier and the quantity

Package 00220-9347-42. 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 Oct 30, 2023.

Indications (excerpt from the label)

Temporarily relieves sinus symptoms due to the common cold or allergies such as: nasal congestion, sinus pain, headache

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)