NDC 43772-0005 Oligo Iodine

Chelidonium Majus, Spongia Tosta, Iodium, Fucus Vesiculosus, Germanium Sesquioxide, Thyroidinum, Calcarea Carbonica

NDC Product Code 43772-0005

NDC Code: 43772-0005

Proprietary Name: Oligo Iodine 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: Chelidonium Majus, Spongia Tosta, Iodium, Fucus Vesiculosus, Germanium Sesquioxide, Thyroidinum, Calcarea Carbonica 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

  • 43772 - Synergy Formulas, Inc.
    • 43772-0005 - Oligo Iodine

NDC 43772-0005-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Oligo Iodine with NDC 43772-0005 is a a human over the counter drug product labeled by Synergy Formulas, Inc.. The generic name of Oligo Iodine is chelidonium majus, spongia tosta, iodium, fucus vesiculosus, germanium sesquioxide, thyroidinum, calcarea carbonica. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Synergy Formulas, Inc.

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.

Oligo Iodine 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.

  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • SPONGIA OFFICINALIS SKELETON, ROASTED 3 [hp_X]/mL
  • IODINE 4 [hp_X]/mL
  • FUCUS VESICULOSUS 6 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • FERROUS IODIDE 12 [hp_X]/mL
  • POTASSIUM IODIDE 12 [hp_X]/mL
  • PULSATILLA VULGARIS 12 [hp_X]/mL
  • CYSTEINE 12 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 12 [hp_X]/mL
  • FUMARIC ACID 12 [hp_X]/mL
  • .ALPHA.-KETOGLUTARIC ACID 12 [hp_X]/mL
  • MANGANESE GLUCONATE 12 [hp_X]/mL
  • BOS TAURUS PITUITARY GLAND 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • SILVER 12 [hp_X]/mL
  • TIN 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • EUGENOL 12 [hp_X]/mL
  • FORMALDEHYDE 12 [hp_X]/mL
  • TITANIUM 12 [hp_X]/mL
  • LIDOCAINE 12 [hp_X]/mL
  • RANCID BEEF 12 [hp_X]/mL
  • VANADIUM 30 [hp_X]/mL
  • BROMINE 30 [hp_X]/mL
  • CALCIUM IODIDE 30 [hp_X]/mL
  • HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED 30 [hp_X]/mL
  • HUMAN COXSACKIEVIRUS B1 8 [hp_C]/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)

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: Synergy Formulas, Inc.
Labeler Code: 43772
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: 04-01-2013 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: 12-31-2019 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.

Oligo Iodine Product Label Images

Oligo Iodine 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

Chelidonium Majus 3X, Spongia Tosta 3X, Iodium 4X, 6X, 12X, Fucus Vesiculosus 6X, 12X, 30X, Germanium Sesquixoide 8X, Thyroidinum (Suis) 8X, 12X, 24X, 30X, 60X, 100X, 200X, Calcarea Carbonica 12X, Ferrum Iodatum 12X, Kali Iodatum 12X, Kali Iodatum 12X, Pulsatilla 12X, Cysteinum 12X, 24X, 30X, Natrum Oxalaceticum 12X, 24X, 30X, Fumaricum Acidum 12X, 24X, 30X, alpha-Ketoglutaricum Acidum 12X, 24X, 30X, Manganese Gluconate 12X, 24X, 30X, Pituitarum Posterium (Bovinum) 12X, 24X, 30X, 60X, 200X, Aurum Metallicum 12X, 30X, 60X, 200X, Molybdenum Metallicum 12X, 30X, 60X, 200X, Palladium Metallicum 12X, 30X, 60X, 200X, Mercurius Solubilis 12X, 30X, 60X, 200X, Argentum Metallicum 12X, 30X, 60X, 200X, Stannum Metallicum 12X, 30X, 60X, 200X, Zincum Metallicum 12X, 30X, 60X, 200X, Cuprum Metallicum 12X, 30X, 60X, 200X, Niccolum Metallicum 12X, 30X, 60X, 200X, Eugenol 12X, 30X, 60X, 200X, Formalinum 12X, 30X, 60X, 200X, Titanium Metallicum 12X, 30X, 60X, 200X, Lidocaine 12X, 30X, 60X, 200X, Pyrogenium 14X, Vanadium Metallicum 30X, 60X, 200X, Bromium 30X, 200X, Calarea Iodata 30X, 200X, Pertussinum 30X, 200X, Coxsackie B1 8C, 12C, 30C, 200C

Indications

For temporary relief of fatigue, muscular weakness, weak pulse, cold hands and feet.  Low blood pressure, nervous tremor, and sensitivity to cold.

Warnings

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.  If pregnant or breast-feeding, ask a health professional before use.  Do not use if tamper evident seal is broken or missing.

Directions

10 drops orally. 3 times a day.  Consult a physician for use in children under 12 years of age.

Inactive Ingredients

Demineralized Water, 25% Ethanol

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away.

Indications And Usage

For temporary relief of fatigue, muscular weakness, weak pulse, cold hands and feet. Low blood pressure, nervous tremor, and sensitivity to cold.

Quesitons

Distributed by:SYNERGY FORMULAS, INC.251 West RoadCampobello, SC  29322

* Please review the disclaimer below.

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