What is NDC 64578-0154?

64578-0154 is the product NDC for Sinus-Tone, Onion 12 [hp_X]/59.1mL + 9 more ingredients liquid, listed with the FDA by Energetix Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Sinus-Tone (Allium cepa, Echinacea, Hydrastis canadensis, Kali bichromicum, Mercurius solubilis, Mercurius sulphuratus ruber, Mucosa nasalis suis, Natrum sulphuricum, Nux moschata, Pulsatilla.).

What is the active ingredient?

Onion, Echinacea, Unspecified, Goldenseal, Potassium dichromate, Mercurius solubilis, Mercuric sulfide, Sus scrofa nasal mucosa, Sodium sulfate, Nutmeg, Pulsatilla vulgaris.

Energetix Corporation, NDC labeler code 64578. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sinus-Tone?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sinus-Tone NDC 64578-0154 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0154Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0154Add 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
64578-0154-1	6457801540164578015401	59.1 mL in 1 BOTTLE, DROPPER (64578-0154-1)Marketed from Oct 19, 2017

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-Tone
Generic name (nonproprietary): allium cepa, echinacea, hydrastis canadensis, kali bichromicum, mercurius solubilis, mercurius sulphuratus ruber, mucosa nasalis suis, natrum sulphuricum, nux moschata, pulsatilla.
Active ingredients: Onion — 12 [hp_X]/59.1mLEchinacea, Unspecified — 4 [hp_X]/59.1mLGoldenseal — 5 [hp_X]/59.1mLPotassium dichromate — 12 [hp_X]/59.1mLMercurius solubilis — 30 [hp_X]/59.1mLMercuric sulfide — 12 [hp_X]/59.1mLSus scrofa nasal mucosa — 9 [hp_X]/59.1mLSodium sulfate — 12 [hp_X]/59.1mLNutmeg — 6 [hp_X]/59.1mLPulsatilla vulgaris — 12 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix CorporationNDC labeler code 64578
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 19, 2017
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 64578-0154_58ca19b2-8935-4b60-e063-6394a90a8a51SPL ID 58ca19b2-8935-4b60-e063-6394a90a8a51SPL set ID e4dc6772-40c7-42af-8531-20b8d1883fb4UNII 492225Q21H, 4N9P6CC1DX, ZW3Z11D0JV, T4423S18FM, 324Y4038G2, ZI0T668SF1, ID3Z1X61WY, 0YPR65R21J, AEE24M3MQ9, I76KB35JEV
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant 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

N464578015401 followed by a unit qualifier and the quantity

Package 64578-0154-01. 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 Aug 11, 2026.

Indications (excerpt from the label)

Uses Temporary relief of sinus congestion, hay fever.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64578-0154

What is NDC 64578-0154?: 64578-0154 is the product NDC for Sinus-Tone, Onion 12 [hp_X]/59.1mL + 9 more ingredients liquid, listed with the FDA by Energetix Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sinus-Tone (Allium cepa, Echinacea, Hydrastis canadensis, Kali bichromicum, Mercurius solubilis, Mercurius sulphuratus ruber, Mucosa nasalis suis, Natrum sulphuricum, Nux moschata, Pulsatilla.).
What is the active ingredient?: Onion, Echinacea, Unspecified, Goldenseal, Potassium dichromate, Mercurius solubilis, Mercuric sulfide, Sus scrofa nasal mucosa, Sodium sulfate, Nutmeg, Pulsatilla vulgaris.
Who is the labeler?: Energetix Corporation, NDC labeler code 64578. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sinus-Tone?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.