What is NDC 83819-608?

83819-608 is the product NDC for dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF, Melaleuca alternifolia whole 8 [hp_X]/30mL; Glycyrrhiza glabra (Licorice) root powder 10 [hp_X]/30mL spray, listed with the FDA by Celcius Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF (Melaleuca alternifolia, Glycyrrhiza Glabra).

What is the active ingredient?

Melaleuca alternifolia whole, Glycyrrhiza glabra (Licorice) root powder.

Celcius Corp., NDC labeler code 83819. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF?

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.

NDC 83819-608

NDC codes

FDA NDC Directory

Product NDC (as listed)83819-608Labeler and product segments. Claims need a package NDC.

Product NDC at billing width83819-0608Add 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
83819-608-03	8381906080383819060803	1 BOTTLE, PLASTIC in 1 CARTON (83819-608-03) / 30 mL in 1 BOTTLE, PLASTICMarketed from May 29, 2026

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): dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF
Generic name (nonproprietary): melaleuca alternifolia, glycyrrhiza glabra
Active ingredients: Melaleuca alternifolia whole — 8 [hp_X]/30mLGlycyrrhiza glabra (Licorice) root powder — 10 [hp_X]/30mL
Dosage form: Spray
Route: Nasal
Labeler: Celcius Corp.NDC labeler code 83819
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 29, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 83819-608_6dc592df-ae5b-4685-bd42-fde9abd99d46SPL ID 6dc592df-ae5b-4685-bd42-fde9abd99d46SPL set ID 2b22b08b-83cf-464c-97ab-7e858fc4e3f0UNII 976KV4FXYF, 2788Z9758HUPC 0199874627021
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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N483819060803 followed by a unit qualifier and the quantity

Package 83819-0608-03. 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 May 5, 2026.

Indications (excerpt from the label)

Uses • temporarily relieves nasal congestion due to a cold, or other upper respiratory allergies • temporarily relieves sinus congestion, breathing and pressure. Helps clear nasal passages : shrinks swollen membranes

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 83819-608

What is NDC 83819-608?: 83819-608 is the product NDC for dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF, Melaleuca alternifolia whole 8 [hp_X]/30mL; Glycyrrhiza glabra (Licorice) root powder 10 [hp_X]/30mL spray, listed with the FDA by Celcius Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF (Melaleuca alternifolia, Glycyrrhiza Glabra).
What is the active ingredient?: Melaleuca alternifolia whole, Glycyrrhiza glabra (Licorice) root powder.
Who is the labeler?: Celcius Corp., NDC labeler code 83819. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF?: 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.

dermveda SINAFLUX ULTRA NATURAL SINUS RELIEF NDC 83819-608