Fucus Complex Liquid
NDC Package 62106-0744-6

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Fucus Complex (fucus vesiculosus, spongia tosta, badiaga) liquids is indicationsHelps promote and maintain normal metabolic functions.DirectionsAdults: Take ten drops two to three times daily or as recommended by your health care practitioner.To be taken 20 minutes away from food.Place drops directly under the tongue or into 1/4 oz. This formulation utilizes a liquid delivery system. Marketed by Seroyal Usa, this product is identified by NDC 62106-0744.

Identification & Billing

NDC Package Code
62106-0744-6
Package Description
1 BOTTLE, GLASS in 1 CARTON / 50 mL in 1 BOTTLE, GLASS
Product Code
11-Digit Billing Format
62106074406

Clinical Specifications

Proprietary Name
Fucus Complex
Non-Proprietary Name
Fucus Vesiculosus, Spongia Tosta, Badiaga
Substance Name
Fucus Vesiculosus; Spongia Officinalis Skeleton, Roasted; Spongilla Lacustris
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Sublingual - Administration beneath the tongue.
Usage Information
IndicationsHelps promote and maintain normal metabolic functions.DirectionsAdults: Take ten drops two to three times daily or as recommended by your health care practitioner.To be taken 20 minutes away from food.Place drops directly under the tongue or into 1/4 oz. of water.Children: Divide dosage by half and follow adult directions.

Regulatory & Marketing

Labeler Name
Seroyal Usa
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
05-08-2015
End Marketing Date
08-31-2026
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 62106-0744-6 identifies a specific commercial package of 1 bottle, glass in 1 carton / 50 ml in 1 bottle, glass of Fucus Complex, a human over the counter drug labeled by Seroyal Usa. This liquid is formulated for sublingual use and contains fucus vesiculosus; spongia officinalis skeleton, roasted; spongilla lacustris 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 Seroyal Usa on May 08, 2015.

How is this Seroyal Usa product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62106074406. 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 (5-4-1)
62106-0744-6
11-Digit CMS (5-4-2)
62106-0744-06

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