Sinus Relief NDC 61727-335

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-335Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0335Add 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
61727-335-21	61727033521	4 g in 1 TUBE (61727-335-21)Marketed from Jul 24, 2012

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): Sinus Relief
Generic name (nonproprietary): asafetida, echinacea angustifolia, calcium sulfide, potassium dichromate, luffa operculata whole, silicon dioxide, sinusitisinum
Active ingredients: Asafetida — 8 [hp_X]/4gEchinacea angustifolia — 12 [hp_X]/4gCalcium sulfide — 8 [hp_X]/4gPotassium dichromate — 18 [hp_X]/4gLuffa operculata whole — 9 [hp_C]/4gSilicon dioxide — 10 [hp_X]/4gSinusitisinum — 18 [hp_X]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 24, 2012
Listing expires: Dec 31, 2026
Identifiers: Product ID 61727-335_7e58bc5a-9e06-3e20-e053-2991aa0a4d35SPL ID 7e58bc5a-9e06-3e20-e053-2991aa0a4d35SPL set ID 84483171-df92-47de-9203-ed02d64fb5fbUNII W9FZA51AS1, VB06AV5US8, 1MBW07J51Q, T4423S18FM, T013HM08S0, ETJ7Z6XBU4, B575563DM5UPC 0361727335210

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461727033521 followed by a unit qualifier and the quantity

Package 61727-0335-21. 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 Dec 31, 2018.

Indications (excerpt from the label)

Indications & Usage: Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)