NDC 69727-0003 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, Nicotinamidum, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Magnesia Phosphorica, Solidago Virgaurea, Graphites

NDC Product Code 69727-0003

NDC Code: 69727-0003

Proprietary Name: Ultra Advantage What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

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, Nicotinamidum, Baryta Carbonica, Calcarea Carbonica, Calcarea Phosphorica, Magnesia Phosphorica, Solidago Virgaurea, Graphites What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 69727 - Elttac Inc Dba Swl

NDC 69727-0003-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Ultra Advantage with NDC 69727-0003 is a a human over the counter drug product labeled by Elttac Inc Dba Swl. The generic name of Ultra Advantage is 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, nicotinamidum, baryta carbonica, calcarea carbonica, calcarea phosphorica, magnesia phosphorica, solidago virgaurea, graphites. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Elttac Inc Dba Swl

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Ultra Advantage Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ARTEMISIA ABROTANUM FLOWERING TOP 8 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE 8 [hp_X]/mL
  • FUCUS VESICULOSUS 8 [hp_X]/mL
  • HELLEBORUS NIGER ROOT 8 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 8 [hp_X]/mL
  • THYMOL 8 [hp_X]/mL
  • THYMUS SERPYLLUM 8 [hp_X]/mL
  • THYROID, BOVINE 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 8 [hp_X]/mL
  • NIACINAMIDE 8 [hp_X]/mL
  • BARIUM CARBONATE 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_X]/mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 12 [hp_X]/mL
  • GRAPHITE 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)
  • GLYCERIN (UNII: PDC6A3C0OX)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Elttac Inc Dba Swl
Labeler Code: 69727
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-03-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Ultra Advantage Product Label Images

Ultra Advantage Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Abrotanum (Artemisia Abrotanum) 8X, Anacardium Orientale 8X, Fucus Vesiculosus 8X, Helleborus Niger 8X, Hypothalamus Suis 8X, Lycopodium Clavatum 8X, Thymolum 8X, Thymus Serpyllum 8X, Thyroidinum (Bovine) 8X, Glandula Suprarenalis Suis 8X, 12X, 16X, Hepar Suis 8X, 12X, 16X, Pancreas Suis 8X, 12X, 16X, Cinchona Officinalis 8X, 32C, Nicotinamidum 8X, 32C, Baryta Carbonica 12X Calcarea Carbonica 12X, Calcarea Phosphorica 12X, Magnesia Phosphorica 12X, Solidago Virgaurea 12X, Graphites 12X, 32C.

Indications:

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.

Warnings:

Stop use and ask your doctor if symptoms persist or worsen.If pregnant or breast-feeding, take only on advice of a healthcare professional.Keep out of reach of children. Contains alcohol. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in a cool dry place.

Keep Out Of Reach Of Children:

Keep out of reach of children. Contains alcohol. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

Shake bottle vigorously 10 times prior to use. Apply 3 sprays under the tongue twice daily, upon awakening and before sleeping. Do not eat, drink, or brush your teeth 5-10 minutes before or after taking this product.

Inactive Ingredients:

Alcohol (20% v/v), glycerin, purified water.

Questions:

Manufactured in the USAwith U.S. and foreign components for:SWL401 W. President George Bush Hwy., #110Richardson, TX, 75080

Package Label Display:

NDC# 69727-0003-1SOZAWEIGHT LOSSULTRA ADVANTAGEWEIGHT LOSS & APPETITE CONTROLHomeopathic Natural RemedyFOR PROFESSIONAL USE ONLY1 FL OZ (30 ML)

* Please review the disclaimer below.