Sinus Relief NDC 57955-9969

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9969Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9969Add 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
57955-9969-2	57955996902	59 mL in 1 BOTTLE, SPRAY (57955-9969-2)Marketed from Mar 10, 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): Sinus Relief
Generic name (nonproprietary): apis mellifica, baptisia tinctoria, colocynthis, hepar sulphuris calcareum, histaminum hydrochloricum, hydrastis canadensis, ignatia amara, kali bichromicum, kali iodatum, lemna minor, mercurius vivus, pulsatilla, rhus tox, sabadilla, sanguinaria, spigelia anth, sticta, teucrium mar and thuja occidentalis.
Active ingredients: Apis mellifera — 10 [hp_X]/59mLBaptisia tinctoria root — 10 [hp_X]/59mLCitrullus colocynthis fruit pulp — 10 [hp_X]/59mLCalcium sulfide — 10 [hp_X]/59mLHistamine dihydrochloride — 10 [hp_X]/59mLGoldenseal — 10 [hp_X]/59mLStrychnos ignatii seed — 10 [hp_X]/59mLPotassium dichromate — 10 [hp_X]/59mLPotassium iodide — 10 [hp_X]/59mLLemna minor whole — 10 [hp_X]/59mLMercury — 10 [hp_X]/59mLPulsatilla vulgaris whole — 10 [hp_X]/59mLToxicodendron pubescens leaf — 10 [hp_X]/59mLSchoenocaulon officinale seed — 10 [hp_X]/59mLSanguinaria canadensis root — 10 [hp_X]/59mLSpigelia anthelmia whole — 10 [hp_X]/59mLLobaria pulmonaria — 10 [hp_X]/59mLTeucrium marum whole — 10 [hp_X]/59mLThuja occidentalis leafy twig — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 57955-9969_1ba0aa13-052b-44d8-9a71-f97a80f6280fSPL ID 1ba0aa13-052b-44d8-9a71-f97a80f6280fSPL set ID a63b09dd-42ed-4413-961b-7c6e08cb93bfUNII 7S82P3R43Z, 5EF0HWI5WU, 23H32AOH17, 1MBW07J51Q, 3POA0Q644U, ZW3Z11D0JV, 1NM3M2487K, T4423S18FM, 1C4QK22F9J, 621HHM46SV, FXS1BY2PGL, I76KB35JEV, 6IO182RP7A, 6NAF1689IO, N9288CD508, WYT05213GE, D1YM0P5Z2T, 10464S0TAA, 1NT28V9397
Pharmacologic class: Standardized Insect Venom 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

N457955996902 followed by a unit qualifier and the quantity

Package 57955-9969-02. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.