Ultra Advantage Liquid
NDC Package 69727-0002-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Ultra Advantage (abrotanum (artemisia abrotanum), anacardium orientale, fucus vesiculosus, helleborus niger, hypothalamus suis, lycopodium clavatum, thymolum, thymus serpyllum, thyroidinum (bovine), glandula suprarenalis suis, hepar suis, pancreas suis, cinchona officinalis, graphites, nicotinamidum, baryta carbonica, calcarea carbonica, calcarea phosphorica, magnesia phosphorica, solidago virgaurea) liquids is for temporary relief of symptoms related to excess appetite, stress, cravings, regulation of fat metabolism, emotional eating & detoxification. This formulation utilizes a liquid delivery system. Marketed by Elttac Inc Dba Swl, this product is identified by NDC 69727-0002.

Identification & Billing

NDC Package Code
69727-0002-1
Package Description
30 mL in 1 BOTTLE, SPRAY
Product Code
69727-0002
11-Digit Billing Format
69727000201

Clinical Specifications

Proprietary Name
Ultra Advantage
Non-Proprietary Name
Abrotanum (artemisia Abrotanum), Anacardium Orientale, Fucus Vesiculosus, Helleborus Niger, Hypothalamus Suis, Lycopodium Clavatum, Thymolum, Thymus Serpyllum, Thyroidinum (bovine), Glandula Suprarenalis Suis, Hepar Suis, Pancreas Suis, Cinchona Officinalis, Graphites, Nicotinamidum, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Magnesia Phosphorica, Solidago Virgaurea
Substance Name
Artemisia Abrotanum Flowering Top; Barium Carbonate; Cinchona Officinalis Bark; Fucus Vesiculosus; Graphite; Helleborus Niger Root; Lycopodium Clavatum Spore; Magnesium Phosphate, Dibasic Trihydrate; Niacinamide; Oyster Shell Calcium Carbonate, Crude; Pork Liver; Semecarpus Anacardium Juice; Solidago Virgaurea Flowering Top; Sus Scrofa Adrenal Gland; Sus Scrofa Hypothalamus; Sus Scrofa Pancreas; Thymol; Thymus Serpyllum; Thyroid, Bovine; Tribasic Calcium Phosphate
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For temporary relief of symptoms related to excess appetite, stress, cravings, regulation of fat metabolism, emotional eating & detoxification. For temporary relief of symptoms related to excess appetite, stress, cravings, regulation of fat metabolism, emotional eating & detoxification.

Regulatory & Marketing

Labeler Name
Elttac Inc Dba Swl
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
12-12-2018
Listing Expiration
12-31-2026
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 69727-0002-1 identifies a specific commercial package of 30 ml in 1 bottle, spray of Ultra Advantage, a human over the counter drug labeled by Elttac Inc Dba Swl. This liquid is formulated for oral use and contains artemisia abrotanum flowering top; barium carbonate; cinchona officinalis bark; fucus vesiculosus; graphite; helleborus niger root; lycopodium clavatum spore; magnesium phosphate, dibasic trihydrate; niacinamide; oyster shell calcium carbonate, crude; pork liver; semecarpus anacardium juice; solidago virgaurea flowering top; sus scrofa adrenal gland; sus scrofa hypothalamus; sus scrofa pancreas; thymol; thymus serpyllum; thyroid, bovine; tribasic calcium phosphate 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 Elttac Inc Dba Swl on December 12, 2018. The current certification is valid through December 31, 2026.

How is this Elttac Inc Dba Swl product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69727000201. 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)
69727-0002-1
11-Digit CMS (5-4-2)
69727-0002-01

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