Dermveda Sinaflux Ultra Natural Sinus Relief Spray
NDC Package 83819-608-03

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Dermveda Sinaflux Ultra Natural Sinus Relief (melaleuca alternifolia, glycyrrhiza glabra) sprays is classified as a

administered via nasal route. This formulation utilizes a spray delivery system. Marketed by Celcius Corp., this product is identified by NDC 83819-608.

Identification & Billing

NDC Package Code
83819-608-03
Package Description
1 BOTTLE, PLASTIC in 1 CARTON / 30 mL in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
83819060803

Clinical Specifications

Proprietary Name
Dermveda Sinaflux Ultra Natural Sinus Relief
Non-Proprietary Name
Melaleuca Alternifolia, Glycyrrhiza Glabra
Substance Name
Glycyrrhiza Glabra (licorice) Root Powder; Melaleuca Alternifolia Whole
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Nasal - Administration to the nose; administered by way of the nose.

Regulatory & Marketing

Labeler Name
Celcius Corp.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
05-29-2026
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 83819-608-03 identifies a specific commercial package of 1 bottle, plastic in 1 carton / 30 ml in 1 bottle, plastic of Dermveda Sinaflux Ultra Natural Sinus Relief, a human over the counter drug labeled by Celcius Corp.. This spray is formulated for nasal use and contains glycyrrhiza glabra (licorice) root powder; melaleuca alternifolia whole as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Celcius Corp. on May 29, 2026. The current certification is valid through December 31, 2027.

How is this Celcius Corp. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83819060803. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
83819-608-03
11-Digit CMS (5-4-2)
83819-0608-03

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.