Sinus Congestion Headache NDC 50845-0263

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0263Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0263Add 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
50845-0263-2	50845026302	1 BOTTLE, SPRAY in 1 PACKAGE (50845-0263-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0263-1)Marketed from Apr 24, 2020

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): Sinus Congestion Headache
Generic name (nonproprietary): antimonium tartaricum, asafoetida, baptisia tinctoria, echinacea (angustifolia), eupatorium perfoliatum, euphorbia pilulifera, hepar sulphuris calcareum, hydrastis canadensis, iodium, kali bichromicum, lachesis mutus, magnesia carbonica, mucosa nasalis suis, pulsatilla (pratensis), pyrogenium, silicea, teucrium marum
Active ingredients: Antimony potassium tartrate — 6 [hp_X]/mLFerula assa-foetida resin — 30 [hp_C]/mLBaptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLEupatorium perfoliatum flowering top — 6 [hp_X]/mLEuphorbia hirta flowering top — 6 [hp_X]/mLCalcium sulfide — 30 [hp_X]/mLGoldenseal — 30 [hp_C]/mLIodine — 200 [hp_C]/mLPotassium dichromate — 30 [hp_X]/mLLachesis muta venom — 200 [hp_C]/mLMagnesium carbonate — 10 [hp_X]/mLSus scrofa nasal mucosa — 12 [hp_X]/mLPulsatilla pratensis whole — 30 [hp_C]/mLRancid beef — 200 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLTeucrium marum whole — 3 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Liddell Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 24, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 50845-0263_6c71b14c-9ef4-47e9-8042-41d95a20453aSPL ID 6c71b14c-9ef4-47e9-8042-41d95a20453aSPL set ID debc7747-8664-4598-a862-e295188c4fcaUNII DL6OZ476V3, W9FZA51AS1, 5EF0HWI5WU, VB06AV5US8, 1W0775VX6E, 6H89ZY31MR, 1MBW07J51Q, ZW3Z11D0JV, 9679TC07X4, T4423S18FM, VSW71SS07I, 0E53J927NA, ID3Z1X61WY, 8E272251DI, 29SUH5R3HU, ETJ7Z6XBU4, 10464S0TAA

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

N450845026302 followed by a unit qualifier and the quantity

Package 50845-0263-02. 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 Nov 4, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve these symptoms associated with sinus congestion: drainage, sinus related headache pain and pressure.** **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)