SinuFix NDC 70163-0030

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0030Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0030Add 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
70163-0030-2	70163003002	1 BOTTLE, DROPPER in 1 CARTON (70163-0030-2) / 30 mL in 1 BOTTLE, DROPPER (70163-0030-1)Marketed from Apr 22, 2026

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): SinuFix
Generic name (nonproprietary): thuja occidentalis, antimonium tartaricum, kali bichromicum, mercurius iodatus ruber, spongia tosta, hepar sulphuris calcareum
Active ingredients: Thuja occidentalis leafy twig — 6 [hp_X]/mLAntimony potassium tartrate — 6 [hp_X]/mLPotassium dichromate — 6 [hp_X]/mLMercuric iodide — 12 [hp_X]/mLSpongia officinalis skeleton, Roasted — 10 [hp_X]/mLCalcium sulfide — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: NaturalCare
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 22, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 70163-0030_fbd27f97-5014-489e-8d3a-1475247f8b4dSPL ID fbd27f97-5014-489e-8d3a-1475247f8b4dSPL set ID 3e2346e7-55a1-416e-b2ef-04d43e40d67fUNII 1NT28V9397, DL6OZ476V3, T4423S18FM, R03O05RB0P, 1PIP394IID, 1MBW07J51QUPC 0371400507018

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

N470163003002 followed by a unit qualifier and the quantity

Package 70163-0030-02. 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 Apr 22, 2026.

Indications (excerpt from the label)

USES: May help temporarily relieve ■ sinus symptoms ■ sinus headache ■ nasal congestion ■ sinus pressure ■ sneezing* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)